TY  - GEN
AU  - Stern,L M
AU  - Mureh,A R
TI  - 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
SN  - 0022-2593
PY  - 1975///1230
KW  - Chromosomes, Human, 16-18
KW  - Disorders of Sex Development
KW  - genetics
KW  - Female
KW  - Humans
KW  - Infant
KW  - Karyotyping
KW  - Pedigree
KW  - Translocation, Genetic
KW  - Trisomy
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1136/jmg.12.3.305
ER  -