PMID- 9738866
OWN - NLM
STAT- MEDLINE
DCOM- 19990115
LR  - 20190905
IS  - 0148-7299 (Print)
IS  - 0148-7299 (Linking)
VI  - 79
IP  - 1
DP  - 1998 Aug 27
TI  - Centric fission of chromosome 9 in a boy with trisomy 9p.
PG  - 35-7
AB  - A centric fission of chromosome 9 was found in a boy with trisomy 9p resulting 
      from a de novo del (9p) and a 9p isochromosome. The patient presented with 
      clinical findings similar to those described in previously reported cases of 
      trisomy 9p. The cytogenetic evaluation and the molecular analysis using 
      fluorescence in situ hybridization (FISH) with specific alphoid probe for 
      chromosome 9 showed a karyotype of 47,XY,+del(9)(q10),+i(9p). We suggest that the 
      mechanism leading to this situation is unusual.
FAU - Concolino, D
AU  - Concolino D
AD  - Department of Pediatrics, Faculty of Medicine, University of Catanzaro, Italy.
FAU - Cinti, R
AU  - Cinti R
FAU - Moricca, M
AU  - Moricca M
FAU - Andria, G
AU  - Andria G
FAU - Strisciuglio, P
AU  - Strisciuglio P
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  - *Chromosomes, Human, Pair 9
MH  - Humans
MH  - Male
MH  - *Trisomy
EDAT- 1998/09/17 02:03
MHDA- 2000/06/20 09:00
CRDT- 1998/09/17 02:03
PHST- 1998/09/17 02:03 [pubmed]
PHST- 2000/06/20 09:00 [medline]
PHST- 1998/09/17 02:03 [entrez]
AID - 10.1002/(SICI)1096-8628(19980827)79:1<35::AID-AJMG9>3.0.CO;2-H [pii]
AID - 10.1002/(sici)1096-8628(19980827)79:1<35::aid-ajmg9>3.0.co;2-h [doi]
PST - ppublish
SO  - Am J Med Genet. 1998 Aug 27;79(1):35-7. doi: 
      10.1002/(sici)1096-8628(19980827)79:1<35::aid-ajmg9>3.0.co;2-h.