Complex glycerol kinase deficiency: Molecular-genetic, cytogenetic, and clinical studies of five Japanese patients-Reference-Cited by-同舟云学术

Complex glycerol kinase deficiency: Molecular-genetic, cytogenetic, and clinical studies of five Japanese patients

Published:1988-11 Issue:3 Volume:31 Page:603-616
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Matsumoto Tadashi,Kondoh Tatsuro,Yoshimoto Masaaki,Fujieda Kenji,Matsuura Nobuo,Matsuda Ichiro,Miike Teruhisa,Yano Koichi,Okuno Akimasa,Aoki Yoshiharu,Murano Ichiro,Toyota Shigeki,Ohnishi Shouju,Niikawa Norio,Opitz John M.,Reynolds James F.

Publisher

Wiley

Subject

Genetics(clinical)

Reference30 articles.

1. CONCORDANCE OF X-LINKED GLYCEROL KINASE DEFICIENCY WITH X-LINKED CONGENITAL ADRENAL HYPOPLASIA

2. Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion

3. Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families.

4. Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studies.

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