Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenita.
about
Glycerol metabolism and the determination of triglycerides--clinical, biochemical and molecular findings in six subjects.Anesthesia for a child suffering from a deletion in the Xp21 loci resulting in Duchenne disease, glycerol kinase deficiency, and congenital adrenal hypoplasia.Isolated glycerol kinase deficiency in a neonate.
P2860
Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenita.
description
1991 nî lūn-bûn
@nan
1991年の論文
@ja
1991年学术文章
@wuu
1991年学术文章
@zh
1991年学术文章
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1991年学术文章
@zh-hans
1991年学术文章
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1991年学术文章
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1991年學術文章
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1991年學術文章
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name
Characterisation of a Xp21 mic ...... adrenal hypoplasia congenita.
@en
Characterisation of a Xp21 mic ...... adrenal hypoplasia congenita.
@nl
type
label
Characterisation of a Xp21 mic ...... adrenal hypoplasia congenita.
@en
Characterisation of a Xp21 mic ...... adrenal hypoplasia congenita.
@nl
prefLabel
Characterisation of a Xp21 mic ...... adrenal hypoplasia congenita.
@en
Characterisation of a Xp21 mic ...... adrenal hypoplasia congenita.
@nl
P2093
P356
P1433
P1476
Characterisation of a Xp21 mic ...... d adrenal hypoplasia congenita
@en
P2093
H Heilbronner
J Schmidtke
R D Wegner
P2888
P304
P356
10.1007/BF00201848
P577
1991-02-01T00:00:00Z