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...

Полное описание

Сохранить в:
Библиографические подробности
Главные авторы: Meitinger, T, Heye, B, Petit, C, Levilliers, J, Golla, A, Moraine, C, Dalla Piccola, B, Sippell, W G, Murken, J, Ballabio, A
Формат: Artigo
Язык:Inglês
Опубликовано: 1990
Предметы:
Research Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683776/
https://ncbi.nlm.nih.gov/pubmed/1977309
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы