TY  - GEN
AU  - Fryns,J P
TI  - Trisomy 9p and tetrasomy 9p: a unique, clinically recognisable syndrome
SN  - 1015-8146
PY  - 1998///1202
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Aneuploidy
KW  - Chromosome Aberrations
KW  - Chromosome Disorders
KW  - Chromosomes, Human, Pair 9
KW  - Craniofacial Abnormalities
KW  - Humans
KW  - Syndrome
KW  - Trisomy
N1  - Publication Type: Letter
ER  -