TY  - GEN
AU  - Lai,C C
AU  - Gorlin,R J
TI  - Trisomy 8 syndrome
SN  - 0009-921X
PY  - 1975///1122
KW  - Abnormalities, Multiple
KW  - etiology
KW  - Adolescent
KW  - Arthrogryposis
KW  - diagnosis
KW  - Bone Diseases, Developmental
KW  - Chromosomes, Human, 6-12 and X
KW  - Cleft Palate
KW  - Deafness
KW  - Diagnosis, Differential
KW  - Dwarfism
KW  - Humans
KW  - Intellectual Disability
KW  - Karyotyping
KW  - Male
KW  - Mosaicism
KW  - Nail-Patella Syndrome
KW  - Osteoporosis
KW  - Syndrome
KW  - Trisomy
N1  - Publication Type: Case Reports; Journal Article
ER  -