Infantile hypophosphatasia: localization within chromosome region 1p36.1-34 and prenatal diagnosis using linked DNA markers.

Linkage analysis was performed on data from Manitoba Mennonite families identified by a proband with infantile hypophosphatasia (HOPS), an autosomal recessive disorder characterized by defective skeletal mineralization. Southern blot analysis of Msp-I-digested DNA from HOPS nuclear families probed w...

Полное описание

Сохранить в:
Библиографические подробности
Главные авторы: Greenberg, C R, Evans, J A, McKendry-Smith, S, Redekopp, S, Haworth, J C, Mulivor, R, Chodirker, B N
Формат: Artigo
Язык:Inglês
Опубликовано: 1990
Предметы:
Research Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC1684978/
https://ncbi.nlm.nih.gov/pubmed/1689104
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы