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Editorial

. 1992 May;50(5):887-91.

Phenotypic heterogeneity and the single gene

G K Suthers, K E Davies

PMID: 1570841
PMCID: PMC1682592

Editorial

Phenotypic heterogeneity and the single gene

G K Suthers et al. Am J Hum Genet. 1992 May.

. 1992 May;50(5):887-91.

Authors

G K Suthers, K E Davies

PMID: 1570841
PMCID: PMC1682592

Erratum in

Am J Hum Genet 1992 Aug;51(2):450
Am J Hum Genet 1992 Jul;51(1):227

No abstract available

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Comment on

Dinucleotide repeat polymorphisms at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenita.
McClatchey AI, Trofatter J, McKenna-Yasek D, Raskind W, Bird T, Pericak-Vance M, Gilchrist J, Arahata K, Radosavljevic D, Worthen HG, et al. McClatchey AI, et al. Am J Hum Genet. 1992 May;50(5):896-901. Am J Hum Genet. 1992. PMID: 1315122 Free PMC article.
Proximal spinal muscular atrophy (SMA) types II and III in the same sibship are not caused by different alleles at the SMA locus on 5q.
Müller B, Melki J, Burlet P, Clerget-Darpoux F. Müller B, et al. Am J Hum Genet. 1992 May;50(5):892-5. Am J Hum Genet. 1992. PMID: 1570842 Free PMC article.

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References

1. J Med Genet. 1992 Mar;29(3):165-70 - PubMed
1. Neuromuscul Disord. 1991;1(2):125-33 - PubMed
1. Hum Genet. 1991 Nov;88(1):71-4 - PubMed
1. Cell. 1991 Nov 29;67(5):1021-7 - PubMed
1. Nature. 1991 Dec 5;354(6352):387-9 - PubMed

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