TY  - GEN
AU  - Pembrey,M
AU  - Baraitser,M
TI  - Recently recognized chromosomal defects of clinical importance
SN  - 0032-5473
PY  - 1987///0219
KW  - Chromosome Aberrations
KW  - diagnosis
KW  - Chromosome Deletion
KW  - Chromosome Disorders
KW  - Female
KW  - Fragile X Syndrome
KW  - genetics
KW  - Genetic Linkage
KW  - Humans
KW  - Male
KW  - Translocation, Genetic
KW  - X Chromosome
N1  - Publication Type: Journal Article; Review
UR  - https://doi.org/10.1136/pgmj.62.724.131
ER  -