Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232.

Kallmann syndrome is a genetically heterogeneous disease characterized by hypogonadotropic hypogonadism and anosmia. Six families in which the disorder followed an X-linked inheritance were investigated by linkage analysis. Diagnostic criteria were uniformly applied and included tests for hypogonado...

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Détails bibliographiques
Auteurs principaux: Meitinger, T, Heye, B, Petit, C, Levilliers, J, Golla, A, Moraine, C, Dalla Piccola, B, Sippell, W G, Murken, J, Ballabio, A
Format: Artigo
Langue:Inglês
Publié: 1990
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683776/
https://ncbi.nlm.nih.gov/pubmed/1977309
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