Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenita. (Q52237907)
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scientific article published in February 1991
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenita. |
scientific article published in February 1991 |
Statements
Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenita (English)
H Heilbronner
R D Wegner
P Fischer
1 February 1991
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