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Genetic heterogeneity in Schwartz-Jampel syndrome: two families with neonatal Schwartz-Jampel syndrome do not map to human chromosome 1p34-p36.1.

Schwartz-Jampel syndrome (SJS) is a rare autosomal recessive disorder characterised by the presence of myotonia with a mask-like face, skeletal dysplasia, and growth retardation. Two types have been defined by the age of manifestation of the symptoms. Linkage of Schwartz-Jampel syndrome to human chr...

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Bibliografske podrobnosti
Main Authors: Brown, K A, al-Gazali, L I, Moynihan, L M, Lench, N J, Markham, A F, Mueller, R F
Format: Artigo
Jezik:English
Izdano: 1997
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051035/
https://ncbi.nlm.nih.gov/pubmed/9279765
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