PMID- 9600733
OWN - NLM
STAT- MEDLINE
DCOM- 19980707
LR  - 20041117
IS  - 0148-7299 (Print)
IS  - 0148-7299 (Linking)
VI  - 77
IP  - 4
DP  - 1998 May 26
TI  - Direct duplication of 9p22-->p24 in a child with duplication 9p syndrome.
PG  - 268-71
AB  - A de novo direct duplication of 9p22-->p24 was shown in a child with a 
      duplication 9p phenotype by GTG banding and fluorescence in situ hybridization 
      (FISH) using a chromosome-9 specific painting probe as well as 6 YAC DNA probes 
      localized to the 9p13-9p23 region. The breakpoints in this patient and previously 
      reported patients suggest that 9p22 may be the critical region for duplication 9p 
      syndrome.
FAU - Fujimoto, A
AU  - Fujimoto A
AD  - Department of Pediatrics, Los Angeles County-University of Southern California 
      Medical Center, and University of Southern California School of Medicine, 90033, 
      USA.
FAU - Lin, M S
AU  - Lin MS
FAU - Schwartz, S
AU  - Schwartz S
LA  - eng
PT  - Case Reports
PT  - Journal Article
PL  - United States
TA  - Am J Med Genet
JT  - American journal of medical genetics
JID - 7708900
SB  - IM
MH  - *Chromosome Aberrations
MH  - Chromosome Banding
MH  - *Chromosome Disorders
MH  - *Chromosomes, Human, Pair 9
MH  - Female
MH  - Humans
MH  - In Situ Hybridization, Fluorescence
MH  - Infant
MH  - Multigene Family
MH  - Syndrome
EDAT- 1998/05/26 02:03
MHDA- 2000/06/20 09:00
CRDT- 1998/05/26 02:03
PHST- 1998/05/26 02:03 [pubmed]
PHST- 2000/06/20 09:00 [medline]
PHST- 1998/05/26 02:03 [entrez]
AID - 10.1002/(SICI)1096-8628(19980526)77:4<268::AID-AJMG3>3.0.CO;2-J [pii]
PST - ppublish
SO  - Am J Med Genet. 1998 May 26;77(4):268-71.