TY  - GEN
AU  - Zackai,E H
AU  - Emanuel,B S
TI  - Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction
SN  - 0148-7299
PY  - 1981///0521
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Chromosomes, Human, 21-22 and Y
KW  - Chromosomes, Human, 6-12 and X
KW  - Female
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Intellectual Disability
KW  - Karyotyping
KW  - Male
KW  - Meiosis
KW  - Pedigree
KW  - Phenotype
KW  - Translocation, Genetic
KW  - Trisomy
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1002/ajmg.1320070412
ER  -