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Indian Journal of Human Genetics
Medknow Publications on behalf of Indian Society of Human Genetics
ISSN: 0971-6866
EISSN: 0971-6866
Vol. 18, No. 1, 2012, pp. 117-118
Bioline Code: hg12022
Full paper language: English
Document type: Case Report
Document available free of charge

Indian Journal of Human Genetics, Vol. 18, No. 1, 2012, pp. 117-118

 en Wolf-Hirschhorn syndrome: A case demonstrated by a cytogenetic study
Pokale, Yamini S.; Jadhav, Ajinkya M. & Kate, Ushang


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.

Chromosomes, chromosome deletion, karyotyping, 4p, micrognathia, Wolf-Hirschhorn syndrome

© Copyright 2012 Indian Journal of Human Genetics.
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