Wolf–Hirschhorn syndrome: A case demonstrated by a cytogenetic study.
Indian J Hum Genet
;
2012 Jan; 18(1): 117-118
Article
Dans Anglais
| IMSEAR
| ID: sea-139456
ABSTRACT
We present a case with a 4p terminal deletion, evidenced in GTG-banded chromosome study. Phenotypic signs described in the classical Wolf–Hirschhorn syndrome were found on clinical examination of our patient.
Texte intégral:
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Indice:
IMSEAR (Asie du Sud-Est)
langue:
Anglais
Texte intégral:
Indian J Hum Genet
Année:
2012
Type:
Article
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