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Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysis.

Mulibrey nanism (MUL) is an autosomal recessive disorder with unknown basic metabolic defect. It is characterized by growth failure of prenatal onset, characteristic dysmorphic features, constrictive pericardium, hepatomegaly as a consequence of constrictive pericardium, yellowish dots in the ocular...

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Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Avela, K, Lipsanen-Nyman, M, Perheentupa, J, Wallgren-Pettersson, C, Marchand, S, Fauré, S, Sistonen, P, de la Chapelle, A, Lehesjoki, A E
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1997
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1712467/
https://ncbi.nlm.nih.gov/pubmed/9106536
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