A RETARDED CHILD WITH A 46XX,3p-q+ CHROMOSOME KARYOTYPE
Author:
Publisher
Wiley
Subject
Psychiatry and Mental health,Clinical Neurology,Neurology,Arts and Humanities (miscellaneous),Rehabilitation
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2788.1974.tb01217.x/fullpdf
Reference26 articles.
1. Identification of translocation chromosomes by quinacrine fluorescence;Breg;.Amer. J. Dis. child.,1972
2. An infant with multiple congenital anomalies and a ring chromosome in group C (X-6-12);Butler;J. med. Genet.,1967
3. A family apparently showing transmission of a translocation between chromosome 3 and one of the X-6-12 or C group;Clarke G. Stevenson;J. med. Genet.,1964
4. An inherited pericentric chromosomal inversion (46, inv. 3 [p−q +]) associated with skeletal anomalies;Cohen;J. Pediat.,1971
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