TY  - GEN
AU  - Sutherland,G R
AU  - Baker,E
TI  - The clinical significance of fragile sites on human chromosomes
SN  - 0009-9163
PY  - 2001///0215
KW  - Chromosome Aberrations
KW  - classification
KW  - Chromosome Disorders
KW  - Chromosome Fragile Sites
KW  - Chromosome Fragility
KW  - genetics
KW  - Fragile X Syndrome
KW  - Genetic Predisposition to Disease
KW  - Humans
KW  - Intellectual Disability
KW  - Prenatal Diagnosis
KW  - X Chromosome
N1  - Publication Type: Journal Article; Review
UR  - https://doi.org/10.1034/j.1399-0004.2000.580301.x
ER  -