-
1
-
-
0024822383
-
The human HOX gene family
-
Acampora D, D'Esposito M, Faiella A, Pannese M, Migliaccio E, Morelli F, Stornaiuolo A, et al (1989) The human HOX gene family. Nucleic Acids Res 17:10385-10402
-
(1989)
Nucleic Acids Res
, vol.17
, pp. 10385-10402
-
-
Acampora, D.1
D'Esposito, M.2
Faiella, A.3
Pannese, M.4
Migliaccio, E.5
Morelli, F.6
Stornaiuolo, A.7
-
2
-
-
0027364749
-
A somatic cell hybrid map of the long arm of human chromosome 17, containing the familial breast cancer locus (BRCA1)
-
Black DM, Nicolai H, Borrow J, Solomon E (1993) A somatic cell hybrid map of the long arm of human chromosome 17, containing the familial breast cancer locus (BRCA1). Am J Hum Genet 52:702-710
-
(1993)
Am J Hum Genet
, vol.52
, pp. 702-710
-
-
Black, D.M.1
Nicolai, H.2
Borrow, J.3
Solomon, E.4
-
3
-
-
0027099864
-
Mox-1 and Mox-2 define a novel homeobox gene subfamily and are differentially expressed during early mesodermal patterning in mouse embryos
-
Candia A, Hu J, Crosby J, Lalley P, Noden D, Nadeau J, Wright C (1992) Mox-1 and Mox-2 define a novel homeobox gene subfamily and are differentially expressed during early mesodermal patterning in mouse embryos. Development 116:1123-1136
-
(1992)
Development
, vol.116
, pp. 1123-1136
-
-
Candia, A.1
Hu, J.2
Crosby, J.3
Lalley, P.4
Noden, D.5
Nadeau, J.6
Wright, C.7
-
4
-
-
0017257594
-
Constrictive pericarditis with dwarfism in two siblings (Mulibrey nanism)
-
Cumming GR, Kerr D, Ferguson CC (1976) Constrictive pericarditis with dwarfism in two siblings (Mulibrey nanism). J Pediatr 88:569-572
-
(1976)
J Pediatr
, vol.88
, pp. 569-572
-
-
Cumming, G.R.1
Kerr, D.2
Ferguson, C.C.3
-
5
-
-
0026532310
-
A dinucleotide repeat polymorphism at the HOX2B locus
-
Deinard AS, Ruano G, Kidd KK (1992) A dinucleotide repeat polymorphism at the HOX2B locus. Nucleic Acids Res 20:1171
-
(1992)
Nucleic Acids Res
, vol.20
, pp. 1171
-
-
Deinard, A.S.1
Ruano, G.2
Kidd, K.K.3
-
6
-
-
0027507885
-
Disease gene mapping in isolated human populations: The example of Finland
-
de la Chapelle A (1993) Disease gene mapping in isolated human populations: the example of Finland. J Med Genet 30:857-865
-
(1993)
J Med Genet
, vol.30
, pp. 857-865
-
-
De La Chapelle, A.1
-
7
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C, Faure S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, et al (1996) A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152-154
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
-
8
-
-
0027980683
-
Isolation of a diverged homeobox gene, MOX1, from the BRCA1 region on 17q21 by solution hybrid capture
-
Futreal PA, Cochran C, Rosenthal J, Miki Y, Swenson J, Hobbs M, Bennet LM, et al (1994) Isolation of a diverged homeobox gene, MOX1, from the BRCA1 region on 17q21 by solution hybrid capture. Hum Mol Genet 3:1359-1364
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1359-1364
-
-
Futreal, P.A.1
Cochran, C.2
Rosenthal, J.3
Miki, Y.4
Swenson, J.5
Hobbs, M.6
Bennet, L.M.7
-
9
-
-
0019524317
-
The genes for growth hormone and chorionic somatomammotropin are on the long arm of human chromosome 17 in region q21-qter
-
George DL, Phillips JA, Francke U, Seeburg PH (1981) The genes for growth hormone and chorionic somatomammotropin are on the long arm of human chromosome 17 in region q21-qter. Hum Genet 57:138-141
-
(1981)
Hum Genet
, vol.57
, pp. 138-141
-
-
George, D.L.1
Phillips, J.A.2
Francke, U.3
Seeburg, P.H.4
-
10
-
-
0028231090
-
The 1993-1994 Généthon human genetic linkage map
-
Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, Millasseau P, Marc S, et al (1994) The 1993-1994 Généthon 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
Millasseau, P.6
Marc, S.7
-
11
-
-
0027211059
-
Antibody deficiency and isolated growth hormone deficiency in a girl with Mulibrey nanism
-
Haraldsson A, van der Burgt CJAM, Weemaes CMR, Otten B, Bakkeren JAJM, Stoelinga GBA (1993) Antibody deficiency and isolated growth hormone deficiency in a girl with Mulibrey nanism. Eur J Pediatr 152:509-512
-
(1993)
Eur J Pediatr
, vol.152
, pp. 509-512
-
-
Haraldsson, A.1
Van Der Burgt, C.J.A.M.2
Weemaes, C.M.R.3
Otten, B.4
Bakkeren, J.A.J.M.5
Stoelinga, G.B.A.6
-
12
-
-
0026949420
-
Linkage disequilibrium mapping in isolated founder populations: Diastrophic dysplasia in Finland
-
Hästbacka J, de la Chapelle A, Kaitila I, Sistonen P, Weaver A, Lander E (1992) Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland. Nat Genet 2:204-211
-
(1992)
Nat Genet
, vol.2
, pp. 204-211
-
-
Hästbacka, J.1
De La Chapelle, A.2
Kaitila, I.3
Sistonen, P.4
Weaver, A.5
Lander, E.6
-
13
-
-
0027978110
-
The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mapping
-
Hästbacka J, de la Chapelle A, Mahtani MM, Clines G, Reeve-Daly MP, Daly M, Hamilton BA, et al (1994) The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping. Cell 78:1073-1087
-
(1994)
Cell
, vol.78
, pp. 1073-1087
-
-
Hästbacka, J.1
De La Chapelle, A.2
Mahtani, M.M.3
Clines, G.4
Reeve-Daly, M.P.5
Daly, M.6
Hamilton, B.A.7
-
14
-
-
0027315230
-
Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLN1) locus at 1p32: Incorporation of linkage disequilibrium in multipoint analysis
-
Hellsten E, Vesa J, Speer MC, Mäkelä TP, Järvelä I, Alitalo K, Ott J, et al (1993) Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLN1) locus at 1p32: incorporation of linkage disequilibrium in multipoint analysis. Genomics 16:720-725
-
(1993)
Genomics
, vol.16
, pp. 720-725
-
-
Hellsten, E.1
Vesa, J.2
Speer, M.C.3
Mäkelä, T.P.4
Järvelä, I.5
Alitalo, K.6
Ott, J.7
-
15
-
-
0029147298
-
Isolation of a novel gene underlying Batten disease, CLN3
-
International Batten Disease Consortium, The (1995) Isolation of a novel gene underlying Batten disease, CLN3. Cell 82: 949-957
-
(1995)
Cell
, vol.82
, pp. 949-957
-
-
-
16
-
-
0028894185
-
Linkage disequilibrium as a gene-mapping tool
-
Jorde LB (1995) Linkage disequilibrium as a gene-mapping tool. Am J Hum Genet 56:11-14
-
(1995)
Am J Hum Genet
, vol.56
, pp. 11-14
-
-
Jorde, L.B.1
-
17
-
-
0028800581
-
Mulibrey nanism: Three additional patients and a review of 39 patients
-
Lapunzina P, Rodriguez JI, de Matteo E, Gracia R, Moreno F (1995) Mulibrey nanism: three additional patients and a review of 39 patients. Am J Med Genet 55:349-355
-
(1995)
Am J Med Genet
, vol.55
, pp. 349-355
-
-
Lapunzina, P.1
Rodriguez, J.I.2
De Matteo, E.3
Gracia, R.4
Moreno, F.5
-
19
-
-
0027236091
-
Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: Linkage disequilibrium allows high resolution mapping
-
Lehesjoki A-E, Koskiniemi M, Norio R, Tirrito S, Sistonen P, Lander E, de la Chapelle A (1993) Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping. Hum Mol Genet 2:1229-1234
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1229-1234
-
-
Lehesjoki, A.-E.1
Koskiniemi, M.2
Norio, R.3
Tirrito, S.4
Sistonen, P.5
Lander, E.6
De La Chapelle, A.7
-
20
-
-
0020052727
-
The efficacy of growth hormone in different types of growth failure: An analysis of 101 cases
-
Lenko HL, Leisti S, Perheentupa J (1982) The efficacy of growth hormone in different types of growth failure: an analysis of 101 cases. Eur J Pediatr 138:241-249
-
(1982)
Eur J Pediatr
, vol.138
, pp. 241-249
-
-
Lenko, H.L.1
Leisti, S.2
Perheentupa, J.3
-
21
-
-
0008913960
-
-
PhD thesis. University of Helsinki, Helsinki
-
Lipsanen-Nyman M (1986) Mulibrey-nanismi. PhD thesis. University of Helsinki, Helsinki
-
(1986)
Mulibrey-nanismi
-
-
Lipsanen-Nyman, M.1
-
22
-
-
0026504525
-
Homeobox genes and axial patterning
-
McGinnis W, Krumlauf R (1992) Homeobox genes and axial patterning. Cell 68:283-302
-
(1992)
Cell
, vol.68
, pp. 283-302
-
-
McGinnis, W.1
Krumlauf, R.2
-
23
-
-
0028940062
-
Batten disease gene, CLN3: Linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes
-
Mitchison HM, O'Rawe AM, Taschner PEM, Sandkuijl LA, Santavuori P, de Vos N, Breuning MH, et al (1995) Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes. Am J Hum Genet 56:654-662
-
(1995)
Am J Hum Genet
, vol.56
, pp. 654-662
-
-
Mitchison, H.M.1
O'Rawe, A.M.2
Taschner, P.E.M.3
Sandkuijl, L.A.4
Santavuori, P.5
De Vos, N.6
Breuning, M.H.7
-
24
-
-
0024513421
-
Maps of linkage and synteny homologies between mouse and man
-
Nadeau JH (1989) Maps of linkage and synteny homologies between mouse and man. Trends Genet 5:82-86
-
(1989)
Trends Genet
, vol.5
, pp. 82-86
-
-
Nadeau, J.H.1
-
25
-
-
0027937794
-
A P1-based physical map of the region from D17S766 to D17S78 containing the breast cancer susceptibility gene BRCA1
-
Neuhausen SL, Swensen J, Miki Y, Liu Q, Tavtigian S, Shattuck-Eidens D, Kamb A, et al (1994) A P1-based physical map of the region from D17S766 to D17S78 containing the breast cancer susceptibility gene BRCA1. Hum Mol Genet 3:1919-1926
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1919-1926
-
-
Neuhausen, S.L.1
Swensen, J.2
Miki, Y.3
Liu, Q.4
Tavtigian, S.5
Shattuck-Eidens, D.6
Kamb, A.7
-
26
-
-
0002739198
-
Diseases of Finland and Scandinavia
-
Rothschild HD (ed). Academic Press, New York
-
Norio R (1981) Diseases of Finland and Scandinavia. In: Rothschild HD (ed) Biocultural aspects of diseases. Academic Press, New York, pp 369-415
-
(1981)
Biocultural Aspects of Diseases
, pp. 369-415
-
-
Norio, R.1
-
27
-
-
0028790963
-
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
-
O'Connell JR, Weeks DE (1995) The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nat Genet 11:402-408
-
(1995)
Nat Genet
, vol.11
, pp. 402-408
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
28
-
-
0039513062
-
Computer-simulation methods in human linkage analysis
-
Ott J (1989) Computer-simulation methods in human linkage analysis. Proc Natl Acad Sci USA 86:4175-4178
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 4175-4178
-
-
Ott, J.1
-
29
-
-
0028980029
-
The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24
-
Paavola P, Salonen R, Weissenbach J, Peltonen L (1995) The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24. Nat Genet 11:213-215
-
(1995)
Nat Genet
, vol.11
, pp. 213-215
-
-
Paavola, P.1
Salonen, R.2
Weissenbach, J.3
Peltonen, L.4
-
30
-
-
13344269666
-
Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)
-
Pennacchio LA, Lehesjoki A-E, Stone N, Willour VL, Virtaneva K, Miao J, D'Amato E, et al (1996) Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1). Science 271:1731-1734
-
(1996)
Science
, vol.271
, pp. 1731-1734
-
-
Pennacchio, L.A.1
Lehesjoki, A.-E.2
Stone, N.3
Willour, V.L.4
Virtaneva, K.5
Miao, J.6
D'Amato, E.7
-
31
-
-
0014899272
-
Mulibrey nanism: Dwarfism with muscle, liver, brain and eye involvement
-
Perheentupa J, Autio S, Leisti S, Raitta C (1970) Mulibrey nanism: dwarfism with muscle, liver, brain and eye involvement. Acta Paediatr Scand Suppl 206:74-75
-
(1970)
Acta Paediatr Scand Suppl
, vol.206
, pp. 74-75
-
-
Perheentupa, J.1
Autio, S.2
Leisti, S.3
Raitta, C.4
-
32
-
-
0015845730
-
Mulibrey-nanism, an autosomal recessive syndrome with pericardial constriction
-
Perheentupa J, Autio S, Leisti S, Raitta C, Tuuteri L (1973) Mulibrey-nanism, an autosomal recessive syndrome with pericardial constriction. Lancet 2:351-355
-
(1973)
Lancet
, vol.2
, pp. 351-355
-
-
Perheentupa, J.1
Autio, S.2
Leisti, S.3
Raitta, C.4
Tuuteri, L.5
-
33
-
-
0027982794
-
Genetic basis of endocrine disease 6: Molecular basis of familial human growth hormone deficiency
-
Phillips JA, Cogan JD (1994) Genetic basis of endocrine disease 6: molecular basis of familial human growth hormone deficiency. J Clin Endocrinol Metab 78:11-16
-
(1994)
J Clin Endocrinol Metab
, vol.78
, pp. 11-16
-
-
Phillips, J.A.1
Cogan, J.D.2
-
35
-
-
0024345383
-
Report of the Committee on the Genetic Constitution of Chromosome 17
-
Solomon E, Baker D (1989) Report of the Committee on the Genetic Constitution of Chromosome 17. Cytogenet Cell Genet 51:319-337
-
(1989)
Cytogenet Cell Genet
, vol.51
, pp. 319-337
-
-
Solomon, E.1
Baker, D.2
-
36
-
-
0027503620
-
Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysis
-
Sulisalo T, Sistonen P, Hästbacka J, Wadelius C, Mäkitie O, de la Chapelle, Kaitila I (1993) Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysis. Nat Genet 3:338-341
-
(1993)
Nat Genet
, vol.3
, pp. 338-341
-
-
Sulisalo, T.1
Sistonen, P.2
Hästbacka, J.3
Wadelius, C.4
Mäkitie, O.5
De La Chapelle6
Kaitila, I.7
-
37
-
-
0015939067
-
So-called Mulibrey nanism with pericardial constriction
-
Thorén C (1973) So-called Mulibrey nanism with pericardial constriction. Lancet 2:731
-
(1973)
Lancet
, vol.2
, pp. 731
-
-
Thorén, C.1
-
38
-
-
0000926583
-
Nonradioactive multiplex procedure for genotyping of microsatellite markers
-
Adolph KW (ed). Academic Press, New York
-
Vignal A, Gyapay G, Hazan J, Nguyen S, Dupraz C, Cheron N, Becuwe N, et al (1993) Nonradioactive multiplex procedure for genotyping of microsatellite markers. In: Adolph KW (ed) Methods in molecular genetics. Vol 1: Gene and chromosome analysis, part A. Academic Press, New York, pp 211-221
-
(1993)
Methods in Molecular Genetics. Vol 1: Gene and Chromosome Analysis
, vol.1
, Issue.PART A
, pp. 211-221
-
-
Vignal, A.1
Gyapay, G.2
Hazan, J.3
Nguyen, S.4
Dupraz, C.5
Cheron, N.6
Becuwe, N.7
-
39
-
-
0029994692
-
Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q
-
Virtaneva K, Miao J, Träskelin A-L, Stone N, Warrington JA, Weissenbach J, Myers RM, et al (1996) Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q. Am J Hum Genet 58:1247-1253
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1247-1253
-
-
Virtaneva, K.1
Miao, J.2
Träskelin, A.-L.3
Stone, N.4
Warrington, J.A.5
Weissenbach, J.6
Myers, R.M.7
-
40
-
-
0017109094
-
Growth failure with pericardial constriction: The syndrome of Mulibrey nanism
-
Voorhess ML, Husson GS, Blackman MS (1976) Growth failure with pericardial constriction: the syndrome of Mulibrey nanism. Am J Dis Child 130:1146-1148
-
(1976)
Am J Dis Child
, vol.130
, pp. 1146-1148
-
-
Voorhess, M.L.1
Husson, G.S.2
Blackman, M.S.3
-
41
-
-
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 44:388-396
-
(1989)
Am J Hum Genet
, vol.44
, pp. 388-396
-
-
Weber, J.L.1
May, P.E.2
-
42
-
-
0000801438
-
SLINK: A general simulation program for linkage analysis
-
Weeks DE, Ott J, Lathrop GM (1990) SLINK: a general simulation program for linkage analysis. Am J Genet Suppl 47:A204
-
(1990)
Am J Genet Suppl
, vol.47
-
-
Weeks, D.E.1
Ott, J.2
Lathrop, G.M.3
-
43
-
-
0026446099
-
A second-generation linkage map of the human genome
-
Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, Millasseau P, Vaysseix G, 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
Millasseau, P.6
Vaysseix, G.7
-
44
-
-
0028073692
-
Localization of disinhibition-dememia-parkinsonism-amyotrophy complex to 17q21-22
-
Willhelmsen KC, Lynch T, Pavlou E, Higgins M, Nygaard TG (1994) Localization of disinhibition-dememia-parkinsonism-amyotrophy complex to 17q21-22. Am J Hum Genet 55:1159-1165
-
(1994)
Am J Hum Genet
, vol.55
, pp. 1159-1165
-
-
Willhelmsen, K.C.1
Lynch, T.2
Pavlou, E.3
Higgins, M.4
Nygaard, T.G.5
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