Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat. [electronic resource]
- Journal of medical genetics Sep 1975
- 305-7 p. digital
Publication Type: Case Reports; Journal Article
0022-2593
10.1136/jmg.12.3.305 doi
Chromosomes, Human, 16-18 Disorders of Sex Development--genetics Female Humans Infant Karyotyping Pedigree Translocation, Genetic Trisomy