Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasia.

Marlhens, F; Chelly, J; Kaplan, J C; Lefrancois, D; Harpey, J P; Dutrillaux, B

Marlhens, F; Chelly, J; Kaplan, J C; Lefrancois, D; Harpey, J P; Dutrillaux, B.

Affiliation

Marlhens F; UA 620 CNRS, Institut Curie, Section de Biologie, Paris, France.

Hum Genet ; 77(4): 379-83, 1987 Dec.

Article in En | MEDLINE | ID: mdl-2891606

Subject(s)

Adrenal Insufficiency/genetics; Chromosome Deletion; Glycerol Kinase/deficiency; Phosphotransferases/deficiency; X Chromosome; Adrenal Insufficiency/congenital; Chromosome Banding; DNA/genetics; Genetic Markers; Humans; Infant, Newborn; Karyotyping; Male; Polymorphism, Restriction Fragment Length

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Phosphotransferases / X Chromosome / Chromosome Deletion / Adrenal Insufficiency / Glycerol Kinase Limits: Humans / Male / Newborn Language: En Journal: Hum Genet Year: 1987 Document type: Article Affiliation country: France Country of publication: Germany

Search on Google

Add to My VHL

XML

PubMed Links