TY  - GEN
AU  - Iwakoshi,Mie
AU  - Okamoto,Nobuhiko
AU  - Harada,Naoki
AU  - Nakamura,Tsuyoshi
AU  - Yamamori,Shunji
AU  - Fujita,Hiroko
AU  - Niikawa,Norio
AU  - Matsumoto,Naomichi
TI  - 9q34.3 deletion syndrome in three unrelated children
SN  - 1552-4825
PY  - 2004///0423
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Adolescent
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosome Disorders
KW  - Chromosomes, Human, 6-12 and X
KW  - Chromosomes, Human, Pair 9
KW  - Face
KW  - abnormalities
KW  - Female
KW  - Heart Defects, Congenital
KW  - Humans
KW  - Infant, Newborn
KW  - Intellectual Disability
KW  - Karyotyping
KW  - Limb Deformities, Congenital
KW  - Male
KW  - Microcephaly
KW  - Monosomy
KW  - Syndrome
KW  - Translocation, Genetic
KW  - Trisomy
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
UR  - https://doi.org/10.1002/ajmg.a.20602
ER  -