PMID- 9109932
OWN - NLM
STAT- MEDLINE
DCOM- 19970501
LR  - 20190816
IS  - 0165-4608 (Print)
IS  - 0165-4608 (Linking)
VI  - 94
IP  - 2
DP  - 1997 Apr
TI  - der(1)t(1;19)(p12;p11): a new nonrandom chromosomal abnormality in 
      myelodysplastic syndrome.
PG  - 85-7
AB  - The der(1)t(1;19)(p12;p11) has not been previously reported in myelodysplastic 
      syndrome (MDS). Fluorescence in situ hybridization (FISH) using chromosome 1- and 
      chromosome 19-specific probes, performed on the bone marrow (BM) cells of this 
      patient confirmed the initial karyotype, i.e., 47,XY,+der(1)t(1;19)(p12;p11).
FAU - Gill, J I
AU  - Gill JI
AD  - Department of Pathology, Tulane University School of Medicine, New Orleans, 
      Louisiana 70112, USA.
FAU - Varela, M
AU  - Varela M
FAU - Tsien, F
AU  - Tsien F
FAU - Krause, J R
AU  - Krause JR
LA  - eng
PT  - Case Reports
PT  - Journal Article
PL  - United States
TA  - Cancer Genet Cytogenet
JT  - Cancer genetics and cytogenetics
JID - 7909240
SB  - IM
MH  - Adult
MH  - Chromosome Aberrations/*genetics
MH  - Chromosome Banding
MH  - Chromosome Disorders
MH  - Chromosomes, Human, Pair 1
MH  - Chromosomes, Human, Pair 19
MH  - Humans
MH  - Male
MH  - Myelodysplastic Syndromes/*genetics
MH  - Translocation, Genetic
EDAT- 1997/04/01 00:00
MHDA- 1997/04/01 00:01
CRDT- 1997/04/01 00:00
PHST- 1997/04/01 00:00 [pubmed]
PHST- 1997/04/01 00:01 [medline]
PHST- 1997/04/01 00:00 [entrez]
AID - S0165-4608(96)00188-4 [pii]
AID - 10.1016/s0165-4608(96)00188-4 [doi]
PST - ppublish
SO  - Cancer Genet Cytogenet. 1997 Apr;94(2):85-7. doi: 10.1016/s0165-4608(96)00188-4.