RT Journal Article
SR Electronic
T1 Trisomy 22 and intersex.
JF Archives of Disease in Childhood - Fetal and Neonatal Edition
JO Arch Dis Child Fetal Neonatal Ed
FD BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health
SP F57
OP F58
DO 10.1136/fn.71.1.F57
VO 71
IS 1
A1 Nicholl, R M
A1 Grimsley, L
A1 Butler, L
A1 Palmer, R W
A1 Rees, H C
A1 Savage, M O
A1 Costeloe, K
YR 1994
UL http://fn.bmj.com/content/71/1/F57.abstract
AB Complete trisomy 22, with or without mosaicism, has been reported as a distinct syndrome. In this report an infant is described who was externally male but with female rudimentary internal organs and whose karyotype was 47,XX+22.