Indian Journal of Human Genetics
Medknow Publications on behalf of Indian Society of Human Genetics
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
© Copyright 2012 Indian Journal of Human Genetics.
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
Alternative site location: http://www.ijhg.com/