-
1
-
-
0035854342
-
Differential timing and control of noncrossover and crossover recombination during meiosis
-
Allers T, Lichten M. 2001. Differential timing and control of noncrossover and crossover recombination during meiosis. Cell 106:47-57
-
(2001)
Cell
, vol.106
, pp. 47-57
-
-
Allers, T.1
Lichten, M.2
-
2
-
-
0032918559
-
Distribution of crossing over on mouse synaptonemal complexes using immunofluorescent localization of MLH1 protein
-
Anderson LK, Reeves A, Webb LM, Ashley T. 1999. Distribution of crossing over on mouse synaptonemal complexes using immunofluorescent localization of MLH1 protein. Genetics 151:1569-79
-
(1999)
Genetics
, vol.151
, pp. 1569-1579
-
-
Anderson, L.K.1
Reeves, A.2
Webb, L.M.3
Ashley, T.4
-
3
-
-
0027209516
-
Allelic diversity at minisatellite MS205 (D16S309): Evidence for polarized variability
-
Armour JA, Harris PC, Jeffreys AJ. 1993. Allelic diversity at minisatellite MS205 (D16S309): evidence for polarized variability. Hum. Mol. Genet. 2:1137-45
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1137-1145
-
-
Armour, J.A.1
Harris, P.C.2
Jeffreys, A.J.3
-
4
-
-
0038052719
-
Hot and cold spots of recombination in the human genome: The reason we should find them and how this can be achieved
-
Arnheim N, Calabrese P, Nordborg M. 2003. Hot and cold spots of recombination in the human genome: the reason we should find them and how this can be achieved. Am. J. Hum. Genet. 73:5-16
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 5-16
-
-
Arnheim, N.1
Calabrese, P.2
Nordborg, M.3
-
5
-
-
0023853503
-
G-band position effects on meiotic synapsis and crossing over
-
Ashley T. 1988. G-band position effects on meiotic synapsis and crossing over. Genetics 118:307-17
-
(1988)
Genetics
, vol.118
, pp. 307-317
-
-
Ashley, T.1
-
6
-
-
0025372442
-
The Gm-Pi linkage in 843 French families: Effect of the alleles Pi Z and Pi S
-
Babron MC, Constans J, Dugoujon JM, Cambon-Thomsen A, Bonaiti-Pellie C. 1990. The Gm-Pi linkage in 843 French families: effect of the alleles Pi Z and Pi S. Ann. Hum. Genet. 54 (Pt. 2):107-13
-
(1990)
Ann. Hum. Genet.
, vol.54
, Issue.PART 2
, pp. 107-113
-
-
Babron, M.C.1
Constans, J.2
Dugoujon, J.M.3
Cambon-Thomsen, A.4
Bonaiti-Pellie, C.5
-
7
-
-
0034194230
-
Crossover breakpoint mapping identifies a subtelomeric hotspot for male meiotic recombination
-
Badge RM, Yardley J, Jeffreys AJ, Armour JA. 2000. Crossover breakpoint mapping identifies a subtelomeric hotspot for male meiotic recombination. Hum. Mol. Genet. 9:1239-44
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1239-1244
-
-
Badge, R.M.1
Yardley, J.2
Jeffreys, A.J.3
Armour, J.A.4
-
8
-
-
8944232867
-
Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over
-
Baker SM, Plug AW, Prolla TA, Bronner CE, Harris AC, et al. 1996. Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over. Nat. Genet. 13:336-42
-
(1996)
Nat. Genet.
, vol.13
, pp. 336-342
-
-
Baker, S.M.1
Plug, A.W.2
Prolla, T.A.3
Bronner, C.E.4
Harris, A.C.5
-
9
-
-
0031829611
-
Crossing over analysis at pachytene in man
-
Barlow AL, Hulten MA. 1998. Crossing over analysis at pachytene in man. Eur. J. Hum. Genet. 6:350-58
-
(1998)
Eur. J. Hum. Genet.
, vol.6
, pp. 350-358
-
-
Barlow, A.L.1
Hulten, M.A.2
-
10
-
-
0000009360
-
A possible influence of the spindle fibre on crossing-over in Drosophila
-
Beadle GW. 1932. A possible influence of the spindle fibre on crossing-over in Drosophila. Proc. Natl. Acad. Sci. USA 18:160-65
-
(1932)
Proc. Natl. Acad. Sci. USA
, vol.18
, pp. 160-165
-
-
Beadle, G.W.1
-
11
-
-
0029013276
-
A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination
-
Blouin JL, Christie DH, Gos A, Lynn A, Morris MA, et al. 1995. A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination. Am. J. Hum. Genet. 57:388-94
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 388-394
-
-
Blouin, J.L.1
Christie, D.H.2
Gos, A.3
Lynn, A.4
Morris, M.A.5
-
12
-
-
0001724069
-
Human Meiosis VIII. Chromosome pairing and formation of the synaptonemal complex in oocytes
-
Bojko M. 1983. Human Meiosis VIII. Chromosome pairing and formation of the synaptonemal complex in oocytes. Carlsberg Res. Commun. 48:457-83
-
(1983)
Carlsberg Res. Commun.
, vol.48
, pp. 457-483
-
-
Bojko, M.1
-
13
-
-
0019302053
-
Construction of a genetic linkage map in man using restriction fragment length polymorphisms
-
Botstein D, White RL, Skolnick M, Davis RW. 1980. Construction of a genetic linkage map in man using restriction fragment length polymorphisms. Am. J. Hum. Genet. 32:314-31
-
(1980)
Am. J. Hum. Genet.
, vol.32
, pp. 314-331
-
-
Botstein, D.1
White, R.L.2
Skolnick, M.3
Davis, R.W.4
-
14
-
-
0032231877
-
Comprehensive human genetic maps: Individual and sex-specific variation in recombination
-
Broman KW, Murray JC, Sheffield VC, White RL, Weber JL. 1998. Comprehensive human genetic maps: individual and sex-specific variation in recombination. Am. J. Hum. Genet. 63:861-69
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 861-869
-
-
Broman, K.W.1
Murray, J.C.2
Sheffield, V.C.3
White, R.L.4
Weber, J.L.5
-
15
-
-
0033855863
-
Meiotic recombination and flanking marker exchange at the highly unstable human minisatellite CEB1 (D2S90)
-
Buard J, Shone AC, Jeffreys AJ. 2000. Meiotic recombination and flanking marker exchange at the highly unstable human minisatellite CEB1 (D2S90). Am. J. Hum. Genet. 67:333-44
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 333-344
-
-
Buard, J.1
Shone, A.C.2
Jeffreys, A.J.3
-
16
-
-
0028238234
-
Complex recombination events at the hypermutable minisatellite CEB1 (D2S90)
-
Buard J, Vergnaud G. 1994. Complex recombination events at the hypermutable minisatellite CEB1 (D2S90). EMBO J. 13:3203-10
-
(1994)
EMBO J.
, vol.13
, pp. 3203-3210
-
-
Buard, J.1
Vergnaud, G.2
-
17
-
-
0025942732
-
Influence of aberrant observations on high-resolution linkage analysis outcomes
-
Buetow KH. 1991. Influence of aberrant observations on high-resolution linkage analysis outcomes. Am. J. Hum. Genet. 49:985-94
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 985-994
-
-
Buetow, K.H.1
-
18
-
-
0028365909
-
Integrated human genome-wide maps constructed using the CEPH reference panel
-
Buetow KH, Weber JL, Ludwigsen S, Scherpbier-Heddema T, Duyk GM, et al. 1994. Integrated human genome-wide maps constructed using the CEPH reference panel. Nat. Genet. 6:391-93
-
(1994)
Nat. Genet.
, vol.6
, pp. 391-393
-
-
Buetow, K.H.1
Weber, J.L.2
Ludwigsen, S.3
Scherpbier-Heddema, T.4
Duyk, G.M.5
-
19
-
-
6844265590
-
Non-disjunction of chromosome 18
-
Bugge M, Collins A, Petersen MB, Fisher J, Brandt C, et al. 1998. Non-disjunction of chromosome 18. Hum. Mol. Genet. 7:661-69
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 661-669
-
-
Bugge, M.1
Collins, A.2
Petersen, M.B.3
Fisher, J.4
Brandt, C.5
-
20
-
-
0019967273
-
Genetic homology and crossing over in the X and Y chromosomes of Mammals
-
Burgoyne PS. 1982. Genetic homology and crossing over in the X and Y chromosomes of Mammals. Hum. Genet. 61:85-90
-
(1982)
Hum. Genet.
, vol.61
, pp. 85-90
-
-
Burgoyne, P.S.1
-
21
-
-
0037370629
-
Using haplotype blocks to map human complex trait loci
-
Cardon LR, Abecasis GR. 2003. Using haplotype blocks to map human complex trait loci. Trends Genet. 19:135-40
-
(2003)
Trends Genet.
, vol.19
, pp. 135-140
-
-
Cardon, L.R.1
Abecasis, G.R.2
-
22
-
-
0027509953
-
DNA deletion associated with hereditary neuropathy with liability to pressure palsies
-
Chance PE, Alderson MK, Leppig KA, Lensch MW, Matsunami N, et al. 1993. DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Cell 72:143-51
-
(1993)
Cell
, vol.72
, pp. 143-151
-
-
Chance, P.E.1
Alderson, M.K.2
Leppig, K.A.3
Lensch, M.W.4
Matsunami, N.5
-
23
-
-
0023039542
-
A model for effective pairing and recombination at meiosis based on early replicating sites (R-bands) along chromosomes
-
Chandley AC. 1986. A model for effective pairing and recombination at meiosis based on early replicating sites (R-bands) along chromosomes. Hum. Genet. 72:50-57
-
(1986)
Hum. Genet.
, vol.72
, pp. 50-57
-
-
Chandley, A.C.1
-
24
-
-
0031909907
-
Why is the centromere so cold?
-
Choo KH. 1998. Why is the centromere so cold? Genome Res. 8:81-82
-
(1998)
Genome Res.
, vol.8
, pp. 81-82
-
-
Choo, K.H.1
-
25
-
-
0027433148
-
A new five-year plan for the U.S. Human Genome Project
-
Collins F, Galas D. 1993. A new five-year plan for the U.S. Human Genome Project. Science 262:43-46
-
(1993)
Science
, vol.262
, pp. 43-46
-
-
Collins, F.1
Galas, D.2
-
26
-
-
0031213897
-
Chiasma interference is blind to centromeres
-
Colombo PC, Jones GH. 1997. Chiasma interference is blind to centromeres. Heredity 79(Pt. 2):214-27
-
(1997)
Heredity
, vol.79
, Issue.PART 2
, pp. 214-227
-
-
Colombo, P.C.1
Jones, G.H.2
-
27
-
-
84984082729
-
The Lutheran-secretor recombination fraction in man: A possible sex difference
-
Cook PJL. 1965. The Lutheran-secretor recombination fraction in man: a possible sex difference. Ann. Hum. Genet. 28:393-97
-
(1965)
Ann. Hum. Genet.
, vol.28
, pp. 393-397
-
-
Cook, P.J.L.1
-
28
-
-
0025280026
-
Centre d'etude du polymorphisme humain (CEPH): Collaborative genetic mapping of the human genome
-
Dausset J, Cann H, Cohen D, Lathrop M, Lalouel JM, White R. 1990. Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome. Genomics 6:575-77
-
(1990)
Genomics
, vol.6
, pp. 575-577
-
-
Dausset, J.1
Cann, H.2
Cohen, D.3
Lathrop, M.4
Lalouel, J.M.5
White, R.6
-
29
-
-
0033711876
-
Bias in multipoint linkage analysis arising from map misspecification
-
Daw EW, Thompson EA, Wijsman EM. 2000. Bias in multipoint linkage analysis arising from map misspecification. Genet. Epidemiol 19:366-80
-
(2000)
Genet. Epidemiol.
, vol.19
, pp. 366-380
-
-
Daw, E.W.1
Thompson, E.A.2
Wijsman, E.M.3
-
30
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C, Faure S, Fizames C, Samson D, Drouot N, et al. 1996. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152-54
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
-
31
-
-
13344287050
-
A comprehensive genetic map of the mouse genome
-
Dietrich WF, Miller J, Steen R, Merchant MA, Damron-Boles D, et al. 1996. A comprehensive genetic map of the mouse genome. Nature 380:149-52
-
(1996)
Nature
, vol.380
, pp. 149-152
-
-
Dietrich, W.F.1
Miller, J.2
Steen, R.3
Merchant, M.A.4
Damron-Boles, D.5
-
32
-
-
0023663060
-
A genetic linkage map of the human genome
-
Donis-Keller H, Green P, Helms C, Cartinhour S, Weiffenbach B, et al. 1987. A genetic linkage map of the human genome. Cell 51:319-37
-
(1987)
Cell
, vol.51
, pp. 319-337
-
-
Donis-Keller, H.1
Green, P.2
Helms, C.3
Cartinhour, S.4
Weiffenbach, B.5
-
33
-
-
0017236514
-
Age trends in human chiasma frequencies and recombination fractions. II. Method for analyzing recombination fractions and applications to the ABO:nail-patella linkage
-
Elston RC, Lange E, Namboodiri KK. 1976. Age trends in human chiasma frequencies and recombination fractions. II. Method for analyzing recombination fractions and applications to the ABO:nail-patella linkage. Am. J. Hum. Genet. 28:69-76
-
(1976)
Am. J. Hum. Genet.
, vol.28
, pp. 69-76
-
-
Elston, R.C.1
Lange, E.2
Namboodiri, K.K.3
-
34
-
-
0035487212
-
Segmental duplications: An "expanding" role in genomic rearrangements
-
Emanuel BS, Shaikh TH. 2001. Segmental duplications: an "expanding" role in genomic rearrangements. Nat. Rev. Genet. 2:791-800
-
(2001)
Nat. Rev. Genet.
, vol.2
, pp. 791-800
-
-
Emanuel, B.S.1
Shaikh, T.H.2
-
35
-
-
0036913535
-
Male mouse recombination maps for each autosome identified by chromosome painting
-
Froenicke L, Anderson LK, Wienberg J, Ashley T. 2002. Male mouse recombination maps for each autosome identified by chromosome painting. Am. J. Hum. Genet. 71:1353-68
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 1353-1368
-
-
Froenicke, L.1
Anderson, L.K.2
Wienberg, J.3
Ashley, T.4
-
36
-
-
0036128504
-
Characteristics of genetic markers and maps for cost-effective genome screens using diallelic markers
-
Goddard KA, Wijsman EM. 2002. Characteristics of genetic markers and maps for cost-effective genome screens using diallelic markers. Genet. Epidemiol. 22:205-20
-
(2002)
Genet. Epidemiol.
, vol.22
, pp. 205-220
-
-
Goddard, K.A.1
Wijsman, E.M.2
-
37
-
-
0038724135
-
The second generation of the International Equine Gene Mapping Workshop half-sibling linkage map
-
Guerin G, Bailey E, Bernoco D, Anderson I, Antczak DF, et al. 2003. The second generation of the International Equine Gene Mapping Workshop half-sibling linkage map. Anim. Genet. 34:161-68
-
(2003)
Anim. Genet.
, vol.34
, pp. 161-168
-
-
Guerin, G.1
Bailey, E.2
Bernoco, D.3
Anderson, I.4
Antczak, D.F.5
-
38
-
-
0028231090
-
The 1993-94 Genethon human genetic linkage map
-
Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, et al. 1994. The 1993-94 Genethon human genetic linkage map. Nat. Genet. 7:246-339
-
(1994)
Nat. Genet.
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
Dib, C.4
Fizames, C.5
-
39
-
-
0029818072
-
Human aneuploidy: Incidence, origin, and etiology
-
Hassold T, Abruzzo M, Adkins K, Griffin D, Merrill M, et al. 1996. Human aneuploidy: incidence, origin, and etiology. Environ. Mol. Mutagen. 28:167-75
-
(1996)
Environ. Mol. Mutagen.
, vol.28
, pp. 167-175
-
-
Hassold, T.1
Abruzzo, M.2
Adkins, K.3
Griffin, D.4
Merrill, M.5
-
40
-
-
0035319804
-
To err (meiotically) is human: The genesis of human aneuploidy
-
Hassold T, Hunt P. 2001. To err (meiotically) is human: the genesis of human aneuploidy. Nat. Rev. Genet. 2:280-91
-
(2001)
Nat. Rev. Genet.
, vol.2
, pp. 280-291
-
-
Hassold, T.1
Hunt, P.2
-
41
-
-
0029118422
-
Recombination and maternal age-dependent nondisjunction: Molecular studies of trisomy 16
-
Hassold T, Merrill M, Adkins K, Freeman S, Sherman S. 1995. Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16. Am. J. Hum. Genet. 57:867-74
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 867-874
-
-
Hassold, T.1
Merrill, M.2
Adkins, K.3
Freeman, S.4
Sherman, S.5
-
42
-
-
0034001512
-
Down syndrome: Genetic recombination and the origin of the extra chromosome 21
-
Hassold T, Sherman S. 2000. Down syndrome: genetic recombination and the origin of the extra chromosome 21. Clin. Genet. 57:95-100
-
(2000)
Clin. Genet.
, vol.57
, pp. 95-100
-
-
Hassold, T.1
Sherman, S.2
-
43
-
-
0033753766
-
Counting cross-overs: Characterizing meiotic recombination in mammals
-
Hassold T, Sherman S, Hunt P. 2000. Counting cross-overs: characterizing meiotic recombination in mammals. Hum. Mol. Genet. 9:2409-19
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2409-2419
-
-
Hassold, T.1
Sherman, S.2
Hunt, P.3
-
45
-
-
0028133503
-
Separation anxiety: The etiology of nondisjunction in flies and people
-
Hawley RS, Frazier JA, Rasooly R. 1994. Separation anxiety: the etiology of nondisjunction in flies and people. Hum. Mol. Genet. 3:1521-28
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1521-1528
-
-
Hawley, R.S.1
Frazier, J.A.2
Rasooly, R.3
-
46
-
-
0027214496
-
Requiem for distributive segregation: Achiasmate segregation in Drosophila females
-
Hawley RS, Theurkauf WE. 1993. Requiem for distributive segregation: achiasmate segregation in Drosophila females. Trends Genet. 9:310-17
-
(1993)
Trends Genet.
, vol.9
, pp. 310-317
-
-
Hawley, R.S.1
Theurkauf, W.E.2
-
47
-
-
0014404553
-
Chiasma frequency and maternal age in mammals
-
Henderson SA, Edwards RG. 1968. Chiasma frequency and maternal age in mammals. Nature 217:22-28
-
(1968)
Nature
, vol.217
, pp. 22-28
-
-
Henderson, S.A.1
Edwards, R.G.2
-
48
-
-
0016192772
-
Chiasma distribution at diakinesis in the normal human male
-
Hulten M. 1974. Chiasma distribution at diakinesis in the normal human male. Hereditas 76:55-78
-
(1974)
Hereditas
, vol.76
, pp. 55-78
-
-
Hulten, M.1
-
49
-
-
0034830932
-
The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes
-
Inoue K, Dewar K, Katsanis N, Reiter LT, Lander ES, et al. 2001. The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes. Genome Res. 11:1018-33
-
(2001)
Genome Res.
, vol.11
, pp. 1018-1033
-
-
Inoue, K.1
Dewar, K.2
Katsanis, N.3
Reiter, L.T.4
Lander, E.S.5
-
52
-
-
0034795550
-
Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex
-
Jeffreys AJ, Kauppi L, Neumann R. 2001. Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex. Nat. Genet. 29:217-22
-
(2001)
Nat. Genet.
, vol.29
, pp. 217-222
-
-
Jeffreys, A.J.1
Kauppi, L.2
Neumann, R.3
-
53
-
-
0032133324
-
High-resolution mapping of crossovers in human sperm defines a minisatellite-associated recombination hotspot
-
Jeffreys AJ, Murray J, Neumann R. 1998. High-resolution mapping of crossovers in human sperm defines a minisatellite-associated recombination hotspot. Mol. Cell 2:267-73
-
(1998)
Mol. Cell
, vol.2
, pp. 267-273
-
-
Jeffreys, A.J.1
Murray, J.2
Neumann, R.3
-
54
-
-
0032528264
-
Repeat instability at human minisatellites arising from meiotic recombination
-
Jeffreys AJ, Neil DL, Neumann R. 1998. Repeat instability at human minisatellites arising from meiotic recombination. EMBO J. 17:4147-57
-
(1998)
EMBO J.
, vol.17
, pp. 4147-4157
-
-
Jeffreys, A.J.1
Neil, D.L.2
Neumann, R.3
-
55
-
-
0034701292
-
High resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot
-
Jeffreys AJ, Ritchie A, Neumann R. 2000. High resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot. Hum. Mol. Genet. 9:725-33
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 725-733
-
-
Jeffreys, A.J.1
Ritchie, A.2
Neumann, R.3
-
56
-
-
0041461913
-
A new framework marker-based linkage map and SDPs for the rat HXB/BXH strain set
-
Jirout M, Krenova D, Kren V, Breen L, Pravenec M, et al. 2003. A new framework marker-based linkage map and SDPs for the rat HXB/BXH strain set. Mamm. Genome 14:537-46
-
(2003)
Mamm. Genome
, vol.14
, pp. 537-546
-
-
Jirout, M.1
Krenova, D.2
Kren, V.3
Breen, L.4
Pravenec, M.5
-
57
-
-
0030140391
-
Chromosome-size dependent control of meiotic recombination in humans
-
Kaback DB. 1996. Chromosome-size dependent control of meiotic recombination in humans. Nat. Genet. 13:20-21
-
(1996)
Nat. Genet.
, vol.13
, pp. 20-21
-
-
Kaback, D.B.1
-
58
-
-
0030989080
-
A second-generation linkage map of the bovine genome
-
Kappes SM, Keele JW, Stone RT, McGraw RA, Sonstegard TS, et al. 1997. A second-generation linkage map of the bovine genome. Genome Res. 7:235-49
-
(1997)
Genome Res.
, vol.7
, pp. 235-249
-
-
Kappes, S.M.1
Keele, J.W.2
Stone, R.T.3
McGraw, R.A.4
Sonstegard, T.S.5
-
59
-
-
12244297072
-
Recombination hotspots rather than population history dominate linkage disequilibrium in the MHC class II region
-
Kauppi L, Sajantila A, Jeffreys AJ. 2003. Recombination hotspots rather than population history dominate linkage disequilibrium in the MHC class II region. Hum. Mol. Genet. 12:33-40
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 33-40
-
-
Kauppi, L.1
Sajantila, A.2
Jeffreys, A.J.3
-
60
-
-
0029775620
-
Meiosis: How could it work?
-
Kleckner N. 1996. Meiosis: How could it work? Proc. Natl. Acad. Sci. USA 93:8167-74
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 8167-8174
-
-
Kleckner, N.1
-
61
-
-
0029852774
-
Spontaneous X chromosome MI and MII nondisjunction events in Drosophila melanogaster oocytes have different recombinational histories
-
Koehler KE, Boulton CL, Collins HE, French RL, Herman KC, et al. 1996. Spontaneous X chromosome MI and MII nondisjunction events in Drosophila melanogaster oocytes have different recombinational histories. Nat. Genet. 14:406-14
-
(1996)
Nat. Genet.
, vol.14
, pp. 406-414
-
-
Koehler, K.E.1
Boulton, C.L.2
Collins, H.E.3
French, R.L.4
Herman, K.C.5
-
62
-
-
18544381909
-
A high-resolution recombination map of the human genome
-
Kong A, Gudbjartsson DF, Sainz J, Jonsdottir GM, Gudjonsson SA, et al. 2002. A high-resolution recombination map of the human genome. Nat. Genet. 31:241-47
-
(2002)
Nat. Genet.
, vol.31
, pp. 241-247
-
-
Kong, A.1
Gudbjartsson, D.F.2
Sainz, J.3
Jonsdottir, G.M.4
Gudjonsson, S.A.5
-
63
-
-
0000732266
-
The estimation of map distances from recombination values
-
Kosambi DD. 1944. The estimation of map distances from recombination values. Ann. Eugen. 12:172-75
-
(1944)
Ann. Eugen.
, vol.12
, pp. 172-175
-
-
Kosambi, D.D.1
-
64
-
-
0030861903
-
The use of a genetic map of biallelic markers in linkage studies
-
Kruglyak L. 1997. The use of a genetic map of biallelic markers in linkage studies. Nat. Genet. 17:21-24
-
(1997)
Nat. Genet.
, vol.17
, pp. 21-24
-
-
Kruglyak, L.1
-
65
-
-
9844220844
-
Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21
-
Lamb NE, Feingold E, Savage A, Avramopoulos D, Freeman S, et al. 1997. Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21. Hum. Mol. Genet. 6:1391-99
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1391-1399
-
-
Lamb, N.E.1
Feingold, E.2
Savage, A.3
Avramopoulos, D.4
Freeman, S.5
-
66
-
-
10544226872
-
Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II
-
Lamb NE, Freeman SB, Savage-Austin A, Pettay D, Taft L, et al. 1996. Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II. Nat. Genet. 14:400-5
-
(1996)
Nat. Genet.
, vol.14
, pp. 400-405
-
-
Lamb, N.E.1
Freeman, S.B.2
Savage-Austin, A.3
Pettay, D.4
Taft, L.5
-
67
-
-
0016760795
-
Age trends in human chiasma frequencies and recombination fractions. I. Chiasma frequencies
-
Lange K, Page BM, Elston RC. 1975. Age trends in human chiasma frequencies and recombination fractions. I. Chiasma frequencies. Am. J. Hum. Genet. 27:410-18
-
(1975)
Am. J. Hum. Genet.
, vol.27
, pp. 410-418
-
-
Lange, K.1
Page, B.M.2
Elston, R.C.3
-
68
-
-
0021885132
-
Further studies on bivalent chiasma frequency in human males with normal karyotypes
-
Laurie DA, Hulten MA. 1985. Further studies on bivalent chiasma frequency in human males with normal karyotypes. Ann. Hum. Genet. 49(Pt. 3): 189-201
-
(1985)
Ann. Hum. Genet.
, vol.49
, Issue.PART 3
, pp. 189-201
-
-
Laurie, D.A.1
Hulten, M.A.2
-
69
-
-
0021800646
-
Further studies on chiasma distribution and interference in the human male
-
Laurie DA, Hulten MA. 1985. Further studies on chiasma distribution and interference in the human male. Ann. Hum. Genet. 49(Pt. 3):203-14
-
(1985)
Ann. Hum. Genet.
, vol.49
, Issue.PART 3
, pp. 203-214
-
-
Laurie, D.A.1
Hulten, M.A.2
-
70
-
-
0019819274
-
Chiasma frequency and distribution in a sample of human males: Chromosomes 1, 2 and 9
-
Laurie DA, Hulten M, Jones GH. 1981. Chiasma frequency and distribution in a sample of human males: chromosomes 1, 2 and 9. Cytogenet. Cell Genet. 31:153-66
-
(1981)
Cytogenet. Cell Genet.
, vol.31
, pp. 153-166
-
-
Laurie, D.A.1
Hulten, M.2
Jones, G.H.3
-
71
-
-
9044240859
-
A de novo case of hereditary neuropathy with a liability to pressure palsies (HNPP) of maternal origin: A new mechanism for deletion in 17p11.2
-
Le Guern E, Gouider R, Ravise N, Lopes J, Tardieu S, et al. 1996. A de novo case of hereditary neuropathy with a liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2. Hum. Mol. Genet. 5:103-6
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 103-106
-
-
Le Guern, E.1
Gouider, R.2
Ravise, N.3
Lopes, J.4
Tardieu, S.5
-
72
-
-
0033929751
-
Evidence for heterogeneity in recombination in the human pseudoautosomal region: High resolution analysis by sperm typing and radiation-hybrid mapping
-
Lien S, Szyda J, Schechinger B, Rappold G, Arnheim N. 2000. Evidence for heterogeneity in recombination in the human pseudoautosomal region: high resolution analysis by sperm typing and radiation-hybrid mapping. Am. J. Hum. Genet. 66:557-66
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 557-566
-
-
Lien, S.1
Szyda, J.2
Schechinger, B.3
Rappold, G.4
Arnheim, N.5
-
73
-
-
0036699091
-
Meiotic arrest and aneuploidy in MLH3-deficient mice
-
Lipkin SM, Moens PB, Wang V, Lenzi M, Shanmugarajah D, et al. 2002. Meiotic arrest and aneuploidy in MLH3-deficient mice. Nat. Genet. 31:385-90
-
(2002)
Nat. Genet.
, vol.31
, pp. 385-390
-
-
Lipkin, S.M.1
Moens, P.B.2
Wang, V.3
Lenzi, M.4
Shanmugarajah, D.5
-
74
-
-
0024514081
-
A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene
-
Litt M, Luty JA. 1989. A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene. Am. J. Hum. Genet. 44:397-401
-
(1989)
Am. J. Hum. Genet.
, vol.44
, pp. 397-401
-
-
Litt, M.1
Luty, J.A.2
-
75
-
-
6844239521
-
Fine mapping of de nova CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination
-
Lopes J, Ravise N, Vanderberghe A, Palau F, Ionasescu V, et al. 1998. Fine mapping of de nova CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination. Hum. Mol. Genet. 7:141-48
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 141-148
-
-
Lopes, J.1
Ravise, N.2
Vanderberghe, A.3
Palau, F.4
Ionasescu, V.5
-
76
-
-
0032695458
-
Homologous DNA exchanges in humans can be explained by the yeast double-strand break model: A study of 17p11.2 rearrangements associated with CMT1A and HNPP
-
Lopes J, Tardieu S, Silander K, Blair I, Vandenberghe A, et al. 1999. Homologous DNA exchanges in humans can be explained by the yeast double-strand break model: a study of 17p11.2 rearrangements associated with CMT1A and HNPP. Hum. Mol. Genet. 8:2285-92
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 2285-2292
-
-
Lopes, J.1
Tardieu, S.2
Silander, K.3
Blair, I.4
Vandenberghe, A.5
-
77
-
-
84984760579
-
Sex-dependent rearrangements resulting in CMT1A and HNPP
-
Lopes J, Vandenberghe A, Tardieu S, Ionasesu V, Levy N, et al. 1997. Sex-dependent rearrangements resulting in CMT1A and HNPP. Nat. Genet. 17:136-37
-
(1997)
Nat. Genet.
, vol.17
, pp. 136-137
-
-
Lopes, J.1
Vandenberghe, A.2
Tardieu, S.3
Ionasesu, V.4
Levy, N.5
-
78
-
-
0033804332
-
Patterns of meiotic recombination on the long arm of human chromosome 21
-
Lynn A, Kashuk C, Petersen MB, Bailey JA, Cox DR, et al. 2000. Patterns of meiotic recombination on the long arm of human chromosome 21. Genome Res. 10:1319-32
-
(2000)
Genome Res.
, vol.10
, pp. 1319-1332
-
-
Lynn, A.1
Kashuk, C.2
Petersen, M.B.3
Bailey, J.A.4
Cox, D.R.5
-
79
-
-
0037150706
-
Covariation of synaptonemal complex length and mammalian meiotic exchange rates
-
Lynn A, Koehler KE, Judis L, Chan ER, Cherry JP, et al. 2002. Covariation of synaptonemal complex length and mammalian meiotic exchange rates. Science 296:2222-25
-
(2002)
Science
, vol.296
, pp. 2222-2225
-
-
Lynn, A.1
Koehler, K.E.2
Judis, L.3
Chan, E.R.4
Cherry, J.P.5
-
80
-
-
0034919163
-
An enhanced linkage map of the sheep genome comprising more than 1000 loci
-
Maddox JF, Davies KP, Crawford AM, Hulme DJ, Vaiman D, et al. 2001. An enhanced linkage map of the sheep genome comprising more than 1000 loci. Genome Res. 11:1275-89
-
(2001)
Genome Res.
, vol.11
, pp. 1275-1289
-
-
Maddox, J.F.1
Davies, K.P.2
Crawford, A.M.3
Hulme, D.J.4
Vaiman, D.5
-
81
-
-
0031911344
-
Physical and genetic mapping of the human X chromosome centromere: Repression of recombination
-
Mahtani MM, Willard HF. 1998. Physical and genetic mapping of the human X chromosome centromere: repression of recombination. Genome Res. 8:100-10
-
(1998)
Genome Res.
, vol.8
, pp. 100-110
-
-
Mahtani, M.M.1
Willard, H.F.2
-
82
-
-
0028343233
-
Automated construction of genetic linkage maps using an expert system (MultiMap): A human genome linkage map
-
Matise TC, Perlin M, Chakravarti A. 1994. Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map. Nat. Genet. 6:384-90
-
(1994)
Nat. Genet.
, vol.6
, pp. 384-390
-
-
Matise, T.C.1
Perlin, M.2
Chakravarti, A.3
-
83
-
-
0041488881
-
A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set
-
Matise TC, Sachidanandam R, Clark AG, Kruglyak L, Wijsman E, et al. 2003. A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set. Am. J. Hum. Genet. 73:271-84
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 271-284
-
-
Matise, T.C.1
Sachidanandam, R.2
Clark, A.G.3
Kruglyak, L.4
Wijsman, E.5
-
84
-
-
0036648248
-
Crossover clustering and rapid decay of linkage disequilibrium in the Xp/Yp pseudoautosomal gene SHOX
-
May CA, Shone AC, Kalaydjieva L, Sajantila A, Jeffreys AJ. 2002. Crossover clustering and rapid decay of linkage disequilibrium in the Xp/Yp pseudoautosomal gene SHOX. Nat. Genet. 31:272-75
-
(2002)
Nat. Genet.
, vol.31
, pp. 272-275
-
-
May, C.A.1
Shone, A.C.2
Kalaydjieva, L.3
Sajantila, A.4
Jeffreys, A.J.5
-
85
-
-
0346284218
-
Second-generation integrated genetic linkage/radiation hybrid maps of the domestic cat (Felis catus)
-
Menotti-Raymond M, David VA, Chen ZQ, Menotti KA, Sun S, et al. 2003. Second-generation integrated genetic linkage/radiation hybrid maps of the domestic cat (Felis catus). J. Hered. 94:95-106
-
(2003)
J. Hered.
, vol.94
, pp. 95-106
-
-
Menotti-Raymond, M.1
David, V.A.2
Chen, Z.Q.3
Menotti, K.A.4
Sun, S.5
-
86
-
-
0033486159
-
A linkage map of 243 DNA markers in an intercross of Gottingen miniature and Meishan pigs
-
Mikawa S, Akita T, Hisamatsu N, Inage Y, Ito Y, et al. 1999. A linkage map of 243 DNA markers in an intercross of Gottingen miniature and Meishan pigs. Anim. Genet. 30:407-17
-
(1999)
Anim. Genet.
, vol.30
, pp. 407-417
-
-
Mikawa, S.1
Akita, T.2
Hisamatsu, N.3
Inage, Y.4
Ito, Y.5
-
87
-
-
0035109310
-
Characterization of rec7, an early meiotic recombination gene in Schizosaccharomyces pombe
-
Molnar M, Parisi S, Kakihara Y, Nojima H, Yamamoto A, et al. 2001. Characterization of rec7, an early meiotic recombination gene in Schizosaccharomyces pombe. Genetics 157:519-32
-
(2001)
Genetics
, vol.157
, pp. 519-532
-
-
Molnar, M.1
Parisi, S.2
Kakihara, Y.3
Nojima, H.4
Yamamoto, A.5
-
88
-
-
0000962735
-
Complete linkage in the second chromosome of the male of Drosophila
-
Morgan TH. 1912. Complete linkage in the second chromosome of the male of Drosophila. Science 36:719-20
-
(1912)
Science
, vol.36
, pp. 719-720
-
-
Morgan, T.H.1
-
89
-
-
0043048571
-
Sequential tests for the detection of linkage
-
Morton NE. 1955. Sequential tests for the detection of linkage. Am. J. Hum. Genet. 7:277-318
-
(1955)
Am. J. Hum. Genet.
, vol.7
, pp. 277-318
-
-
Morton, N.E.1
-
90
-
-
0033015206
-
Comparative sequence analysis of human minisatellites showing meiotic repeat instability
-
Murray J, Buard J, Neil DL, Yeramian E, Tamaki K, et al. 1999. Comparative sequence analysis of human minisatellites showing meiotic repeat instability. Genome Res. 9:130-36
-
(1999)
Genome Res.
, vol.9
, pp. 130-136
-
-
Murray, J.1
Buard, J.2
Neil, D.L.3
Yeramian, E.4
Tamaki, K.5
-
91
-
-
0027942568
-
A comprehensive human linkage map with centimorgan density
-
Cooperative Human Linkage Center (CHLC)
-
Murray JC, Buetow KH, Weber JL, Ludwigsen S, Scherpbier-Heddema T, et al. 1994. A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC). Science 265:2049-54
-
(1994)
Science
, vol.265
, pp. 2049-2054
-
-
Murray, J.C.1
Buetow, K.H.2
Weber, J.L.3
Ludwigsen, S.4
Scherpbier-Heddema, T.5
-
92
-
-
0036889393
-
Variation in recombination rate across the genome: Evidence and implications
-
Nachman MW. 2002. Variation in recombination rate across the genome: evidence and implications. Curr. Opin. Genet. Dev. 12:657-63
-
(2002)
Curr. Opin. Genet. Dev.
, vol.12
, pp. 657-663
-
-
Nachman, M.W.1
-
93
-
-
0032964876
-
A second-generation genetic linkage map of the domestic dog, Canis familiaris
-
Neff MW, Broman KW, Mellersh CS, Ray K, Acland GM, et al. 1999. A second-generation genetic linkage map of the domestic dog, Canis familiaris. Genetics 151:803-20
-
(1999)
Genetics
, vol.151
, pp. 803-820
-
-
Neff, M.W.1
Broman, K.W.2
Mellersh, C.S.3
Ray, K.4
Acland, G.M.5
-
94
-
-
0026774858
-
A comprehensive genetic linkage map of the human genome
-
NIH/CEPH Collab. Mapping Group. 1992. A comprehensive genetic linkage map of the human genome. Science 258:67-86
-
(1992)
Science
, vol.258
, pp. 67-86
-
-
-
95
-
-
0036468808
-
Linkage disequilibrium: What history has to tell us
-
Nordborg M, Tavaré S. 2002. Linkage disequilibrium: what history has to tell us. Trends Genet. 18:83-90
-
(2002)
Trends Genet.
, vol.18
, pp. 83-90
-
-
Nordborg, M.1
Tavaré, S.2
-
96
-
-
0030340606
-
Meiotic nondisjunction does the two-step
-
Orr-Weaver T. 1996. Meiotic nondisjunction does the two-step. Nat. Genet. 14:374-76
-
(1996)
Nat. Genet.
, vol.14
, pp. 374-376
-
-
Orr-Weaver, T.1
-
97
-
-
0028840395
-
Meiosis in Drosophila: Seeing is believing
-
Orr-Weaver TL. 1995. Meiosis in Drosophila: seeing is believing. Proc. Natl. Acad. Sci. USA 92:10443-49
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 10443-10449
-
-
Orr-Weaver, T.L.1
-
99
-
-
0021083003
-
Chiasma-derived genetic lengths and recombination fractions: A reciprocal translocation 46,XY,t(1;22) (q32;q13)
-
Palmer RW, Hulten MA. 1983. Chiasma-derived genetic lengths and recombination fractions: a reciprocal translocation 46,XY,t(1;22) (q32;q13). Ann. Hum. Genet. 47(Pt. 4):299-310
-
(1983)
Ann. Hum. Genet.
, vol.47
, Issue.PART 4
, pp. 299-310
-
-
Palmer, R.W.1
Hulten, M.A.2
-
100
-
-
0035345013
-
Meiotic recombination hot spots and cold spots
-
Petes TD. 2001. Meiotic recombination hot spots and cold spots. Nat. Rev. Genet. 2:360-69
-
(2001)
Nat. Rev. Genet.
, vol.2
, pp. 360-369
-
-
Petes, T.D.1
-
101
-
-
0037459072
-
Un menage a quatre: The molecular biology of chromosome segregation in meiosis
-
Petronczki M, Siomos MF, Nasmyth K. 2003. Un menage a quatre: the molecular biology of chromosome segregation in meiosis. Cell 112:423-40
-
(2003)
Cell
, vol.112
, pp. 423-440
-
-
Petronczki, M.1
Siomos, M.F.2
Nasmyth, K.3
-
102
-
-
0026058844
-
A test of the production line hypothesis of mammalian oogenesis
-
Polani PE, Crolla JA. 1991. A test of the production line hypothesis of mammalian oogenesis. Hum. Genet. 88:64-70
-
(1991)
Hum. Genet.
, vol.88
, pp. 64-70
-
-
Polani, P.E.1
Crolla, J.A.2
-
103
-
-
0002739523
-
Human Meiosis II: Chromosome pairing and recombination nodules in human spermatocytes
-
Rasmussen SW, Holm PB. 1978. Human Meiosis II: chromosome pairing and recombination nodules in human spermatocytes. Carlsberg Res. Commun. 43:275-327
-
(1978)
Carlsberg Res. Commun.
, vol.43
, pp. 275-327
-
-
Rasmussen, S.W.1
Holm, P.B.2
-
104
-
-
84984084531
-
Male and female recombination fractions for the nail-patella:ABO linkage in man
-
Renwick JH, Schulze J. 1965. Male and female recombination fractions for the nail-patella:ABO linkage in man. Ann. Hum. Genet. 28:379-92
-
(1965)
Ann. Hum. Genet.
, vol.28
, pp. 379-392
-
-
Renwick, J.H.1
Schulze, J.2
-
105
-
-
7144260410
-
Maternal meiosis I non-disjunction of chromosome 15: Dependence of the maternal age effect on level of recombination
-
Robinson WP, Kuchinka BD, Bernasconi F, Petersen MB, Schulze A, et al. 1998. Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination. Hum. Mol. Genet. 7:1011-19
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1011-1019
-
-
Robinson, W.P.1
Kuchinka, B.D.2
Bernasconi, F.3
Petersen, M.B.4
Schulze, A.5
-
106
-
-
0028082214
-
The yeast med1 mutant undergoes both meiotic homolog nondisjunction and precocious separation of sister chromatids
-
Rockmill B, Roeder GS. 1994. The yeast med1 mutant undergoes both meiotic homolog nondisjunction and precocious separation of sister chromatids. Genetics 136:65-74
-
(1994)
Genetics
, vol.136
, pp. 65-74
-
-
Rockmill, B.1
Roeder, G.S.2
-
107
-
-
0025221073
-
Chromosome synapsis and genetic recombination
-
Roeder GS. 1990. Chromosome synapsis and genetic recombination. Trends Genet. 6:385-89
-
(1990)
Trends Genet.
, vol.6
, pp. 385-389
-
-
Roeder, G.S.1
-
108
-
-
0030767256
-
Meiotic chromosomes: It takes two to tango
-
Roeder GS. 1997. Meiotic chromosomes: it takes two to tango. Genes Dev. 11:2600-21
-
(1997)
Genes Dev.
, vol.11
, pp. 2600-2621
-
-
Roeder, G.S.1
-
109
-
-
0034253791
-
A genetic linkage map of the baboon (Papio hamadryas) genome based on human microsatellite polymorphisms
-
Rogers J, Mahaney MC, Witte SM, Nair S, Newman D, et al. 2000. A genetic linkage map of the baboon (Papio hamadryas) genome based on human microsatellite polymorphisms. Genomics 67:237-47
-
(2000)
Genomics
, vol.67
, pp. 237-247
-
-
Rogers, J.1
Mahaney, M.C.2
Witte, S.M.3
Nair, S.4
Newman, D.5
-
110
-
-
0025014992
-
An interspersed repeated sequence specific for human subtelomeric regions
-
Rouyer F, de la Chapelle A, Andersson M, Weissenbach J. 1990. An interspersed repeated sequence specific for human subtelomeric regions. EMBO J. 9:505-14
-
(1990)
EMBO J.
, vol.9
, pp. 505-514
-
-
Rouyer, F.1
De La Chapelle, A.2
Andersson, M.3
Weissenbach, J.4
-
111
-
-
10744220154
-
Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion
-
Saitta SC, Harris SE, Gaeth AP, Driscoll DA, McDonald-McGinn DM, et al. 2004. Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion. Hum. Mol. Genet. 13:417-28
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 417-428
-
-
Saitta, S.C.1
Harris, S.E.2
Gaeth, A.P.3
Driscoll, D.A.4
McDonald-McGinn, D.M.5
-
112
-
-
7344224406
-
Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans
-
Savage AR, Petersen MB, Pettay D, Taft L, Allran K, et al. 1998. Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans. Hum. Mol. Genet. 7:1221-27
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1221-1227
-
-
Savage, A.R.1
Petersen, M.B.2
Pettay, D.3
Taft, L.4
Allran, K.5
-
113
-
-
0031761948
-
Comparative gene mapping: A fine-scale survey of chromosome rearrangements between ruminants and humans
-
Schibler L, Vaiman D, Oustry A, Giraud-Delville C, Cribiu EP. 1998. Comparative gene mapping: a fine-scale survey of chromosome rearrangements between ruminants and humans. Genome Res. 8:901-15
-
(1998)
Genome Res.
, vol.8
, pp. 901-915
-
-
Schibler, L.1
Vaiman, D.2
Oustry, A.3
Giraud-Delville, C.4
Cribiu, E.P.5
-
114
-
-
5444239910
-
An association between meiotic recombination and advancing maternal age for trisomy 21
-
Sherman S, Feingold E, Lamb N. 2003. An association between meiotic recombination and advancing maternal age for trisomy 21. Am. J. Hum. Genet. 73(Suppl.):A311
-
(2003)
Am. J. Hum. Genet.
, vol.73
, Issue.SUPPL.
-
-
Sherman, S.1
Feingold, E.2
Lamb, N.3
-
115
-
-
0036077159
-
Absence of age effect on meiotic recombination between human X and Y chromosomes
-
Shi Q, Spriggs E, Field LL, Rademaker A, Ko E, et al. 2002. Absence of age effect on meiotic recombination between human X and Y chromosomes. Am. J. Hum. Genet. 71:254-61
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 254-261
-
-
Shi, Q.1
Spriggs, E.2
Field, L.L.3
Rademaker, A.4
Ko, E.5
-
116
-
-
0036186038
-
Sex-specific recombination rates in zebrafish (Danio rerio)
-
Singer A, Perlman H, Yan Y, Walker C, Corley-Smith G, et al. 2002. Sex-specific recombination rates in zebrafish (Danio rerio). Genetics 160:649-57
-
(2002)
Genetics
, vol.160
, pp. 649-657
-
-
Singer, A.1
Perlman, H.2
Yan, Y.3
Walker, C.4
Corley-Smith, G.5
-
117
-
-
0036234001
-
A deer (subfamily Cervinae) genetic linkage map and the evolution of ruminant genomes
-
Slate J, Van Stijn TC, Anderson RM, McEwan KM, Maqbool NJ, et al. 2002. A deer (subfamily Cervinae) genetic linkage map and the evolution of ruminant genomes. Genetics 160:1587-97
-
(2002)
Genetics
, vol.160
, pp. 1587-1597
-
-
Slate, J.1
Van Stijn, T.C.2
Anderson, R.M.3
McEwan, K.M.4
Maqbool, N.J.5
-
119
-
-
0036468807
-
Genome architecture, rearrangements and genomic disorders
-
Stankiewicz P, Lupski JR. 2002. Genome architecture, rearrangements and genomic disorders. Trends Genet. 18:74-82
-
(2002)
Trends Genet.
, vol.18
, pp. 74-82
-
-
Stankiewicz, P.1
Lupski, J.R.2
-
120
-
-
0038067849
-
Genome architecture catalyzes nonrecurrent chromosomal rearrangements
-
Stankiewicz P, Shaw CJ, Dapper JD, Wakui K, Shaffer LG, et al. 2003. Genome architecture catalyzes nonrecurrent chromosomal rearrangements. Am. J. Hum. Genet. 72:1101-16
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 1101-1116
-
-
Stankiewicz, P.1
Shaw, C.J.2
Dapper, J.D.3
Wakui, K.4
Shaffer, L.G.5
-
121
-
-
0020541955
-
The double-strand-break repair model for recombination
-
Szostak JW, Orr-Weaver TL, Rothstein RJ. 1983. The double-strand-break repair model for recombination. Cell 33:25-35
-
(1983)
Cell
, vol.33
, pp. 25-35
-
-
Szostak, J.W.1
Orr-Weaver, T.L.2
Rothstein, R.J.3
-
122
-
-
0025653870
-
Detailed genetic linkage map of human chromosome 21: Patterns of recombination according to age and sex
-
Tanzi RE, Haines JL, Gusella JF. 1990. Detailed genetic linkage map of human chromosome 21: patterns of recombination according to age and sex. Prog. Clin. Biol. Res. 360:15-26
-
(1990)
Prog. Clin. Biol. Res.
, vol.360
, pp. 15-26
-
-
Tanzi, R.E.1
Haines, J.L.2
Gusella, J.F.3
-
123
-
-
0026514890
-
A genetic linkage map of human chromosome 21: Analysis of recombination as a function of sex and age
-
Tanzi RE, Watkins PC, Stewart GD, Wexler NS, Gusella JF, Haines JL. 1992. A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and age. Am. J. Hum. Genet. 50:551-58
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 551-558
-
-
Tanzi, R.E.1
Watkins, P.C.2
Stewart, G.D.3
Wexler, N.S.4
Gusella, J.F.5
Haines, J.L.6
-
124
-
-
0036091625
-
Patterns of meiotic recombination in human fetal oocytes
-
Tease C, Hartshorne GM, Hulten MA. 2002. Patterns of meiotic recombination in human fetal oocytes. Am. J. Hum. Genet. 70:1469-79
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 1469-1479
-
-
Tease, C.1
Hartshorne, G.M.2
Hulten, M.A.3
-
125
-
-
0033777149
-
A reinvestigation of non-disjunction resulting in 47. XXY males of paternal origin
-
Thomas NS, Collins AR, Hassold TJ, Jacobs PA. 2000. A reinvestigation of non-disjunction resulting in 47, XXY males of paternal origin. Eur. J. Hum. Genet. 8:805-8
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 805-808
-
-
Thomas, N.S.1
Collins, A.R.2
Hassold, T.J.3
Jacobs, P.A.4
-
126
-
-
0035253363
-
Maternal sex chromosome non-disjunction: Evidence for X chromosome-specific risk factors
-
Thomas NS, Ennis S, Sharp AJ, Durkie M, Hassold TJ, et al. 2001. Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factors. Hum. Mol. Genet. 10:243-50
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 243-250
-
-
Thomas, N.S.1
Ennis, S.2
Sharp, A.J.3
Durkie, M.4
Hassold, T.J.5
-
127
-
-
0029163591
-
A collection of ordered tetranucleotide-repeat markers from the human genome
-
Utah Marker Dev. Group. 1995. A collection of ordered tetranucleotide-repeat markers from the human genome. Am. J. Hum. Genet. 57:619-28
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 619-628
-
-
-
128
-
-
0023236677
-
Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome
-
Warren AC, Chakravarti A, Wong C, Slaugenhaupt SA, Halloran SL, et al. 1987. Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome. Science 237:652-54
-
(1987)
Science
, vol.237
, pp. 652-654
-
-
Warren, A.C.1
Chakravarti, A.2
Wong, C.3
Slaugenhaupt, S.A.4
Halloran, S.L.5
-
129
-
-
0036649518
-
The Iceland map
-
Weber JL. 2002. The Iceland map. Nat. Genet. 31:225-26
-
(2002)
Nat. Genet.
, vol.31
, pp. 225-226
-
-
Weber, J.L.1
-
130
-
-
0035228946
-
Genotyping for human whole-genome scans: Past, present, and future
-
Weber JL, Broman KW. 2001. Genotyping for human whole-genome scans: past, present, and future. Adv. Genet. 42:77-96
-
(2001)
Adv. Genet.
, vol.42
, pp. 77-96
-
-
Weber, J.L.1
Broman, K.W.2
-
131
-
-
0024582686
-
Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction
-
Weber JL, May PE. 1989. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am. J. Hum. Genet. 44:388-96
-
(1989)
Am. J. Hum. Genet.
, vol.44
, pp. 388-396
-
-
Weber, J.L.1
May, P.E.2
-
132
-
-
0037364995
-
Inactivation of Exonuclease 1 in mice results in DNA mismatch repair defects, increased cancer susceptibility, and male and female infertility
-
Wei K, Clark AB, Wong E, Kane MF, Mazur DJ, et al. 2003. Inactivation of Exonuclease 1 in mice results in DNA mismatch repair defects, increased cancer susceptibility, and male and female infertility. Genes Dev. 17:603-14
-
(2003)
Genes Dev.
, vol.17
, pp. 603-614
-
-
Wei, K.1
Clark, A.B.2
Wong, E.3
Kane, M.F.4
Mazur, D.J.5
-
133
-
-
0026446099
-
A second-generation linkage map of the human genome
-
Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, et al. 1992. A second-generation linkage map of the human genome. Nature 359:794-801
-
(1992)
Nature
, vol.359
, pp. 794-801
-
-
Weissenbach, J.1
Gyapay, G.2
Dib, C.3
Vignal, A.4
Morissette, J.5
-
134
-
-
0033926575
-
Equivalence of single- and multilocus markers: Power to detect linkage with composite markers derived from biallelic loci
-
Wilson AF, Sorant AJ. 2000. Equivalence of single- and multilocus markers: power to detect linkage with composite markers derived from biallelic loci. Am. J. Hum. Genet. 66:1610-15
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 1610-1615
-
-
Wilson, A.F.1
Sorant, A.J.2
-
135
-
-
0035865094
-
Comparison of human genetic and sequence-based physical maps
-
Yu A, Zhao C, Fan Y, Jang W, Mungall AJ, et al. 2001. Comparison of human genetic and sequence-based physical maps. Nature 409:951-53
-
(2001)
Nature
, vol.409
, pp. 951-953
-
-
Yu, A.1
Zhao, C.2
Fan, Y.3
Jang, W.4
Mungall, A.J.5
-
136
-
-
0029852086
-
Individual variation in recombination among human males
-
Yu J, Lazzeroni L, Qin J, Huang MM, Navidi W, et al. 1996. Individual variation in recombination among human males. Am. J. Hum. Genet. 59:1186-92
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 1186-1192
-
-
Yu, J.1
Lazzeroni, L.2
Qin, J.3
Huang, M.M.4
Navidi, W.5
-
137
-
-
0033975302
-
The murine SCP3 gene is required for synaptonemal complex assembly, chromosome synapsis, and male fertility
-
Yuan L, Liu JG, Zhao J, Brundell E, Daneholt B, Hoog C. 2000. The murine SCP3 gene is required for synaptonemal complex assembly, chromosome synapsis, and male fertility. Mol. Cell 5:73-83
-
(2000)
Mol. Cell
, vol.5
, pp. 73-83
-
-
Yuan, L.1
Liu, J.G.2
Zhao, J.3
Brundell, E.4
Daneholt, B.5
Hoog, C.6
-
138
-
-
0036742496
-
The first comprehensive genetic linkage map of a marsupial: The tammar wallaby (Macropus eugenii)
-
Zenger KR, McKenzie LM, Cooper DW. 2002. The first comprehensive genetic linkage map of a marsupial: the tammar wallaby (Macropus eugenii). Genetics 162:321-30
-
(2002)
Genetics
, vol.162
, pp. 321-330
-
-
Zenger, K.R.1
McKenzie, L.M.2
Cooper, D.W.3
-
139
-
-
0028810669
-
Mutant rec-1 eliminates the meiotic pattern of crossing over in Caenorhabditis elegans
-
Zetka MC, Rose AM. 1995. Mutant rec-1 eliminates the meiotic pattern of crossing over in Caenorhabditis elegans. Genetics 141:1339-49
-
(1995)
Genetics
, vol.141
, pp. 1339-1349
-
-
Zetka, M.C.1
Rose, A.M.2
-
140
-
-
0033368701
-
Meiotic chromosomes: Integrating structure and function
-
Zickler D, Klecker N. 1999. Meiotic chromosomes: integrating structure and function. Annu. Rev. Genet. 33:603-754
-
(1999)
Annu. Rev. Genet.
, vol.33
, pp. 603-754
-
-
Zickler, D.1
Klecker, N.2
|