A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-).

This publication has 6 references indexed in Scilit:

• [Partial trisomy C through a familial translocation t(Cq+;Cq-)].
  1968
• A FAMILIAL 4/5 RECIPROCAL TRANSLOCATION RESULTTING IN PARTIAL TRISOMY B
  1965
• Meiotic and Mitotic Studies of a Familial Reciprocal Translocation Between Two Autosomes of Group 6–12
  Cytogenetic and Genome Research, 1965
• MATERNAL TRANSMISSION OF A NEW GROUP-C(6/9) CHROMOSOMAL SYNDROME
  The Lancet, 1964
• TURNER'S SYNDROME WITH SECONDARY AMENORRHOEA AND SEX CHROMOSOME MOSAICISM
  Acta Endocrinologica, 1964
• TRITIATED THYMIDINE INCORPORATION IN AN ISOCHROMOSOME FOR THE LONG ARM OF THE X CHROMOSOME IN MAN
  The Lancet, 1963