TY  - GEN
AU  - Courtens,W
AU  - Perlmutter,N
AU  - Dan,B
AU  - Vamos,E
TI  - New syndrome or severe expression of Gordon syndrome? A case report
SN  - 0962-8827
PY  - 1997///0326
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Genetic Linkage
KW  - Humans
KW  - Infant, Newborn
KW  - Male
KW  - Syndrome
KW  - X Chromosome
N1  - Publication Type: Case Reports; Journal Article
ER  -