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Xp11.21 Google OMIM Orphanet PubMed Wikipedia Faciogenital dysplasia *Gene map locus Xp11.21 AAS Aarskog syndrome Aarskog-Scott syndrome FGDY Faciodigitogenital syndrome Mental retardation, X-linked nonsyndromic [Clinical features: short stature; facial dysmorphism; shawl scrotum] [Inheritance: X-linked recessive] |
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Aarskog syndrome |
Aarskog syndrome |
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Indian Pediatrics |
Indian Pediatrics |
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Edited by Aldo Campana,
March 14, 2010
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