-
1
-
-
85031595922
-
-
for distances for D9S172-D9S60
-
Genetic Location Database, http://cedar.genetics.soton.ac.uk/ public_html/ (for distances for D9S172-D9S60)
-
-
-
-
2
-
-
85031597738
-
-
for autosomal recessive LGMD [MIM 254110]
-
Online Mendelian Inheritance in Man (OMIM), http:// www.ncbi.nlm.nih.gov/Omim (for autosomal recessive LGMD [MIM 254110])
-
-
-
-
3
-
-
0028326542
-
A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p
-
Bashir R, Strachan T, Keers S, Stephenson A, Mahjneh I, Marconi G, Nashef L, et al (1994) A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p. Hum Mol Genet 3:455-457
-
(1994)
Hum Mol Genet
, vol.3
, pp. 455-457
-
-
Bashir, R.1
Strachan, T.2
Keers, S.3
Stephenson, A.4
Mahjneh, I.5
Marconi, G.6
Nashef, L.7
-
4
-
-
0031972889
-
Automatic selection of loop breakers for genetic linkage analysis
-
Becker A, Geiger D, Schaffet AA (1998) Automatic selection of loop breakers for genetic linkage analysis. Hum Hered 48:49-60
-
(1998)
Hum Hered
, vol.48
, pp. 49-60
-
-
Becker, A.1
Geiger, D.2
Schaffet, A.A.3
-
5
-
-
0028971219
-
β-Sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex
-
Bönnemann CG, Modi R, Noguchi S, Mizuno Y, Yoshida M, Gussoni E, McNally EM, et al (1995) β-Sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex. Nat Genet 11: 266-272
-
(1995)
Nat Genet
, vol.11
, pp. 266-272
-
-
Bönnemann, C.G.1
Modi, R.2
Noguchi, S.3
Mizuno, Y.4
Yoshida, M.5
Gussoni, E.6
McNally, E.M.7
-
6
-
-
10544252688
-
Genomic screening for β-sarcoglycan gene mutations: Missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)
-
Bönnemann CG, Passos-Bueno MR, McNally EM, Vainzof M, Moreira ED, Marie SK, Pavanello RCM, et al (1996) Genomic screening for β-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E). Hum Mol Genet 5:1953-1961
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1953-1961
-
-
Bönnemann, C.G.1
Passos-Bueno, M.R.2
McNally, E.M.3
Vainzof, M.4
Moreira, E.D.5
Marie, S.K.6
Pavanello, R.C.M.7
-
7
-
-
0028835527
-
Diagnostic criteria for the limb-girdle muscular dystrophies: Report of the ENMC consortium on limb-girdle dystrophies
-
Bushby KMD (1995) Diagnostic criteria for the limb-girdle muscular dystrophies: report of the ENMC consortium on limb-girdle dystrophies. Neuromusc Disord 5:71-74
-
(1995)
Neuromusc Disord
, vol.5
, pp. 71-74
-
-
Bushby, K.M.D.1
-
8
-
-
0028851065
-
Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15
-
Carmi R, Rokhlina T, Kwitek-Black AE, Elbedour K, Nishimura D, Stone EM, Sheffield VC (1995) Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15. Hum Mol Genet 4:9-13
-
(1995)
Hum Mol Genet
, vol.4
, pp. 9-13
-
-
Carmi, R.1
Rokhlina, T.2
Kwitek-Black, A.E.3
Elbedour, K.4
Nishimura, D.5
Stone, E.M.6
Sheffield, V.C.7
-
9
-
-
0029988255
-
A metric map of humans: 23,500 loci in 850 bands
-
Collins A, Frezal J, Teague J, Morton NE (1996) A metric map of humans: 23,500 loci in 850 bands. Proc Natl Acad Sci USA 93:14771-14775
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 14771-14775
-
-
Collins, A.1
Frezal, J.2
Teague, J.3
Morton, N.E.4
-
11
-
-
0024542131
-
Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren
-
Fujiwara TM, Morgan K, Schwartz RH, Doherty RA, Miller SR, Klinger K, Stanislovitis P, et al (1989) Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren. Am J Hum Genet 44: 327-337
-
(1989)
Am J Hum Genet
, vol.44
, pp. 327-337
-
-
Fujiwara, T.M.1
Morgan, K.2
Schwartz, R.H.3
Doherty, R.A.4
Miller, S.R.5
Klinger, K.6
Stanislovitis, P.7
-
12
-
-
0023242308
-
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21
-
Greenberg CR, Hamerton JL, Nigli M, Wrogemann K (1987) DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21. Am J Hum Genet 41:128-137
-
(1987)
Am J Hum Genet
, vol.41
, pp. 128-137
-
-
Greenberg, C.R.1
Hamerton, J.L.2
Nigli, M.3
Wrogemann, K.4
-
13
-
-
0030893619
-
Molecular genetic evidence of clinical heterogeneity in Fukuyama-type congenital muscular dystrophy
-
Kondo-Iida E, Saito K, Tanaka H, Tsuji S, Ishihara T, Osawa M, Fukuyama Y, et al (1997) Molecular genetic evidence of clinical heterogeneity in Fukuyama-type congenital muscular dystrophy. Hum Genet 99:427-432
-
(1997)
Hum Genet
, vol.99
, pp. 427-432
-
-
Kondo-Iida, E.1
Saito, K.2
Tanaka, H.3
Tsuji, S.4
Ishihara, T.5
Osawa, M.6
Fukuyama, Y.7
-
14
-
-
0029886532
-
Parametric and nonparametric linkage analysis: A unified multipoint approach
-
Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES (1996) Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet 58:1347-1363
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1347-1363
-
-
Kruglyak, L.1
Daly, M.J.2
Reeve-Daly, M.P.3
Lander, E.S.4
-
15
-
-
0021344005
-
Easy calculations of lod scores and genetic risks on small computers
-
Lathrop GM, Lalouel JM (1984) Easy calculations of lod scores and genetic risks on small computers. Am J Hum Genet 36:460-465
-
(1984)
Am J Hum Genet
, vol.36
, pp. 460-465
-
-
Lathrop, G.M.1
Lalouel, J.M.2
-
17
-
-
0022646961
-
Construction of human linkage maps: Likelihood calculations for multilocus linkage analysis
-
Lathrop GM, Lalouel JM, White RL (1986) Construction of human linkage maps: likelihood calculations for multilocus linkage analysis. Genet Epidemiol 3:39-52
-
(1986)
Genet Epidemiol
, vol.3
, pp. 39-52
-
-
Lathrop, G.M.1
Lalouel, J.M.2
White, R.L.3
-
18
-
-
0028971221
-
β-Sarcoglycan: Characterization and role in limb-girdle muscular dystrophy linked to 4q12
-
Lim LE, Duclos F, Broux O, Bourg N, Sunada Y, Allamand V, Meyer J, et al (1995) β-Sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12. Nat Genet 11:257-265
-
(1995)
Nat Genet
, vol.11
, pp. 257-265
-
-
Lim, L.E.1
Duclos, F.2
Broux, O.3
Bourg, N.4
Sunada, Y.5
Allamand, V.6
Meyer, J.7
-
19
-
-
0027998371
-
Ubiquinone biosynthesis in eukaryotic cells: Tissue distribution of mRNA encoding 3,4-dihydroxy-5-polyprenylbenzoate methyltransferase in the rat and mapping of the COQ3 gene to mouse chromosome 4
-
Marbois BN, Xia YR, Lusis AJ, Clarke CF (1994) Ubiquinone biosynthesis in eukaryotic cells: tissue distribution of mRNA encoding 3,4-dihydroxy-5-polyprenylbenzoate methyltransferase in the rat and mapping of the COQ3 gene to mouse chromosome 4. Arch Biochem Biophys 313:83-88
-
(1994)
Arch Biochem Biophys
, vol.313
, pp. 83-88
-
-
Marbois, B.N.1
Xia, Y.R.2
Lusis, A.J.3
Clarke, C.F.4
-
20
-
-
0030724952
-
Absence of integrin a7 causes a novel form of muscular dystrophy
-
Mayer U, Saher G, Fassler R, Bornemann A, Echtermeyer F, von der Mark H, Miosge N, et al (1997) Absence of integrin a7 causes a novel form of muscular dystrophy. Nat Genet 17:318-323
-
(1997)
Nat Genet
, vol.17
, pp. 318-323
-
-
Mayer, U.1
Saher, G.2
Fassler, R.3
Bornemann, A.4
Echtermeyer, F.5
Von Der Mark, H.6
Miosge, N.7
-
22
-
-
0030882270
-
Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23
-
Messina DN, Speer MC, Pericak-Vance MA, McNally EM (1997) Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23. Am J Hum Genet 61:909-917
-
(1997)
Am J Hum Genet
, vol.61
, pp. 909-917
-
-
Messina, D.N.1
Speer, M.C.2
Pericak-Vance, M.3
McNally, E.M.4
-
23
-
-
0031920515
-
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy
-
Minetti C, Sotgia F, Bruno C, Scartezzini P, Broda P, Bado M, Masetti E, et al (1998) Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy. Nat Genet 18:365-368
-
(1998)
Nat Genet
, vol.18
, pp. 365-368
-
-
Minetti, C.1
Sotgia, F.2
Bruno, C.3
Scartezzini, P.4
Broda, P.5
Bado, M.6
Masetti, E.7
-
24
-
-
0031106122
-
YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31
-
Miyake M, Nakahori Y, Matsushita I, Kobayashi K, Mizuno K, Hirai M, Kanazawa I, et al (1997) YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31. Genomics 40:284-293
-
(1997)
Genomics
, vol.40
, pp. 284-293
-
-
Miyake, M.1
Nakahori, Y.2
Matsushita, I.3
Kobayashi, K.4
Mizuno, K.5
Hirai, M.6
Kanazawa, I.7
-
25
-
-
0030765309
-
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12
-
Moreira ES, Vainzof M, Marie SK, Sertié AL, Zatz M, Passos-Bueno MR (1997) The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12. Am J Hum Genet 61:151-159
-
(1997)
Am J Hum Genet
, vol.61
, pp. 151-159
-
-
Moreira, E.S.1
Vainzof, M.2
Marie, S.K.3
Sertié, A.L.4
Zatz, M.5
Passos-Bueno, M.R.6
-
26
-
-
0027722978
-
Chromosomal localization of the mouse titin gene and its relation to "muscular dystrophy with myositis" and nebulin genes on chromosome 2
-
Muller-Seitz M, Kaupmann K, Labeit S, Jockusch H (1993) Chromosomal localization of the mouse titin gene and its relation to "muscular dystrophy with myositis" and nebulin genes on chromosome 2. Genomics 18:559-561
-
(1993)
Genomics
, vol.18
, pp. 559-561
-
-
Muller-Seitz, M.1
Kaupmann, K.2
Labeit, S.3
Jockusch, H.4
-
27
-
-
0029816797
-
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ-sarcoglycan gene
-
Nigro V, de Sa Moreira E, Piluso G, Vainzof M, Belsito A, Politano L, Puca AA, et al (1996) Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ-sarcoglycan gene. Nat Genet 14:195-198
-
(1996)
Nat Genet
, vol.14
, pp. 195-198
-
-
Nigro, V.1
De Sa Moreira, E.2
Piluso, G.3
Vainzof, M.4
Belsito, A.5
Politano, L.6
Puca, A.A.7
-
28
-
-
0028883973
-
Mutations in the dystrophin-associated protein γ-sarcoglycan in chromosome 13 muscular dystrophy
-
Noguchi S, McNally EM, Ben Othmane K, Hagiwara Y, Mizuno Y, Yoshida M, Yamamoto H, et al (1995) Mutations in the dystrophin-associated protein γ-sarcoglycan in chromosome 13 muscular dystrophy. Science 270:819-822
-
(1995)
Science
, vol.270
, pp. 819-822
-
-
Noguchi, S.1
McNally, E.M.2
Ben Othmane, K.3
Hagiwara, Y.4
Mizuno, Y.5
Yoshida, M.6
Yamamoto, H.7
-
29
-
-
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
-
30
-
-
0030008373
-
Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD
-
Passos-Bueno MR, Moreira ES, Vainzof M, Marie SK, Zatz M (1996) Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD. Hum Mol Genet 5:815-820
-
(1996)
Hum Mol Genet
, vol.5
, pp. 815-820
-
-
Passos-Bueno, M.R.1
Moreira, E.S.2
Vainzof, M.3
Marie, S.K.4
Zatz, M.5
-
31
-
-
0028905205
-
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A
-
Richard I, Broux O, Allamand V, Fougerousse F, Chiannilkulchai N, Bourg N, Brenguier L, et al (1995) Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A. Cell 81:27-40
-
(1995)
Cell
, vol.81
, pp. 27-40
-
-
Richard, I.1
Broux, O.2
Allamand, V.3
Fougerousse, F.4
Chiannilkulchai, N.5
Bourg, N.6
Brenguier, L.7
-
32
-
-
0028146869
-
Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy
-
Roberds SL, Leturcq F, Allamand V, Piccolo F, Jeanpierre M, Anderson RD, Lim LE, et al (1994) Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy. Cell 78:625-633
-
(1994)
Cell
, vol.78
, pp. 625-633
-
-
Roberds, S.L.1
Leturcq, F.2
Allamand, V.3
Piccolo, F.4
Jeanpierre, M.5
Anderson, R.D.6
Lim, L.E.7
-
33
-
-
0028229122
-
Recombinations in individuals homozygous by descent localize the Friedreich ataxia locus in a cloned 450-kb interval
-
Rodius F, Duclos F, Wrogemann K, Le Paslier D, Ougen P, Billault A, Belal S, et al (1994) Recombinations in individuals homozygous by descent localize the Friedreich ataxia locus in a cloned 450-kb interval. Am J Hum Genet 54: 1050-1059
-
(1994)
Am J Hum Genet
, vol.54
, pp. 1050-1059
-
-
Rodius, F.1
Duclos, F.2
Wrogemann, K.3
Le Paslier, D.4
Ougen, P.5
Billault, A.6
Belal, S.7
-
34
-
-
0029946879
-
Faster linkage analysis computations for pedigrees with loops or unused alleles
-
Schäffer AA (1996) Faster linkage analysis computations for pedigrees with loops or unused alleles. Hum Hered 46: 226-235
-
(1996)
Hum Hered
, vol.46
, pp. 226-235
-
-
Schäffer, A.A.1
-
36
-
-
10244230901
-
A gene map of the human genome
-
Schuler GD, Boguski MS, Stewart EA, Stein LD, Gyapay G, Rice K, White RE, et al (1996) A gene map of the human genome. Science 274:540-546
-
(1996)
Science
, vol.274
, pp. 540-546
-
-
Schuler, G.D.1
Boguski, M.S.2
Stewart, E.A.3
Stein, L.D.4
Gyapay, G.5
Rice, K.6
White, R.E.7
-
37
-
-
0028000502
-
Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping
-
Sheffield VC, Carmi R, Kwitek-Black A, Rokhlina T, Nishimura D, Duyk GM, Elbedour K, et al (1994) Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping. Hum Mol Genet 3:1331-1335
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1331-1335
-
-
Sheffield, V.C.1
Carmi, R.2
Kwitek-Black, A.3
Rokhlina, T.4
Nishimura, D.5
Duyk, G.M.6
Elbedour, K.7
-
38
-
-
0017259056
-
Autosomal recessive muscular dystrophy in Manitoba Hutterites
-
Shokeir MHK, Kobrinsky NL (1976) Autosomal recessive muscular dystrophy in Manitoba Hutterites. Clin Genet 9: 197-202
-
(1976)
Clin Genet
, vol.9
, pp. 197-202
-
-
Shokeir, M.H.K.1
Kobrinsky, N.L.2
-
39
-
-
0003008512
-
Vacillans, a neurological mutant in the house mouse linked with brown
-
Sirlin JL (1956) Vacillans, a neurological mutant in the house mouse linked with brown. J Genet 54:42-48
-
(1956)
J Genet
, vol.54
, pp. 42-48
-
-
Sirlin, J.L.1
-
40
-
-
84966152677
-
Location of vacillans in linkage group VIII of the house mouse
-
Sirlin JL (1957) Location of vacillans in linkage group VIII of the house mouse. Heredity 11:259-260
-
(1957)
Heredity
, vol.11
, pp. 259-260
-
-
Sirlin, J.L.1
-
41
-
-
0026524275
-
Friedreich ataxia in Louisiana Acadians: Demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes
-
Sirugo G, Keats B, Fujita R, Duclos F, Purohit K, Koenig M, Mandel JL (1992) Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes. Am J Hum Genet 50: 559-566
-
(1992)
Am J Hum Genet
, vol.50
, pp. 559-566
-
-
Sirugo, G.1
Keats, B.2
Fujita, R.3
Duclos, F.4
Purohit, K.5
Koenig, M.6
Mandel, J.L.7
-
42
-
-
0028788563
-
Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy
-
Speer MC, Gilchrist JM, Chutkow JG, McMichael R, Westbrook CA, Stajich JM, Jorgenson EM, et al (1995) Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy. Am J Hum Genet 57:1371-1376
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1371-1376
-
-
Speer, M.C.1
Gilchrist, J.M.2
Chutkow, J.G.3
McMichael, R.4
Westbrook, C.A.5
Stajich, J.M.6
Jorgenson, E.M.7
-
43
-
-
0026690760
-
Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: Linkage of an autosomal dominant form to chromosome 5q
-
Speer MC, Yamaoka LH, Gilchrist JH, Gaskell CP, Stajich JM, Vance JM, Kazantsev A, et al (1992) Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q. Am J Hum Genet 50:1211-1217
-
(1992)
Am J Hum Genet
, vol.50
, pp. 1211-1217
-
-
Speer, M.C.1
Yamaoka, L.H.2
Gilchrist, J.H.3
Gaskell, C.P.4
Stajich, J.M.5
Vance, J.M.6
Kazantsev, A.7
-
44
-
-
0030909575
-
Muscular dystrophies and the dystrophin glycoprotein complex
-
Straub V, Campbell KP (1997) Muscular dystrophies and the dystrophin glycoprotein complex. Curr Opin Neurol 10: 168-175
-
(1997)
Curr Opin Neurol
, vol.10
, pp. 168-175
-
-
Straub, V.1
Campbell, K.P.2
-
46
-
-
0028114849
-
Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: Evidence for strong linkage disequilibrium
-
Toda T, Ikegawa S, Okui K, Kondo E, Saito K, Fukuyama Y, Yoshioka M, et al (1994) Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: evidence for strong linkage disequilibrium. Am J Hum Genet 55:946-950
-
(1994)
Am J Hum Genet
, vol.55
, pp. 946-950
-
-
Toda, T.1
Ikegawa, S.2
Okui, K.3
Kondo, E.4
Saito, K.5
Fukuyama, Y.6
Yoshioka, M.7
-
47
-
-
19244362767
-
Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb
-
Toda T, Miyake M, Kobayashi K, Mizuno K, Saito K, Osawa M, Nakamura Y, et al (1996) Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb. Am J Hum Genet 59:1313-1320
-
(1996)
Am J Hum Genet
, vol.59
, pp. 1313-1320
-
-
Toda, T.1
Miyake, M.2
Kobayashi, K.3
Mizuno, K.4
Saito, K.5
Osawa, M.6
Nakamura, Y.7
-
48
-
-
0027364850
-
Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33
-
Toda T, Segawa M, Nomura Y, Nonaka I, Masuda K, Ishihara T, Suzuki M, et al (1993) Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33. Nat Genet 5:283-286
-
(1993)
Nat Genet
, vol.5
, pp. 283-286
-
-
Toda, T.1
Segawa, M.2
Nomura, Y.3
Nonaka, I.4
Masuda, K.5
Ishihara, T.6
Suzuki, M.7
-
49
-
-
0030898109
-
Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21
-
van der Kooi AJ, van Meegen M, Ledderhof TM, McNally EM, de Visser M, Bolhuis PA (1997) Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21. Am J Hum Genet 60:891-895
-
(1997)
Am J Hum Genet
, vol.60
, pp. 891-895
-
-
Van Der Kooi, A.J.1
Van Meegen, M.2
Ledderhof, T.M.3
McNally, E.M.4
De Visser, M.5
Bolhuis, P.A.6
-
50
-
-
0027161022
-
Mutation of human short tandem repeats
-
Weber JL, Wong C (1993) Mutation of human short tandem repeats. Hum Mol Genet 2:1123-1128
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1123-1128
-
-
Weber, J.L.1
Wong, C.2
-
51
-
-
0030752595
-
Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD loci
-
Weiler T, Greenberg CR, Nylen E, Morgan K, Fujiwara TM, Crumley MJ, Zelinski T, et al (1997) Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD loci. Am J Med Genet 72:363-368
-
(1997)
Am J Med Genet
, vol.72
, pp. 363-368
-
-
Weiler, T.1
Greenberg, C.R.2
Nylen, E.3
Morgan, K.4
Fujiwara, T.M.5
Crumley, M.J.6
Zelinski, T.7
-
52
-
-
0026072689
-
The use of DNA restriction fragment length polymorphisms in conjunction with blood group serology
-
Zelinski T (1991) The use of DNA restriction fragment length polymorphisms in conjunction with blood group serology. Transfusion 31:762-770
-
(1991)
Transfusion
, vol.31
, pp. 762-770
-
-
Zelinski, T.1
|