PMID- 1424236
OWN - NLM
STAT- MEDLINE
DCOM- 19921202
LR  - 20190816
IS  - 0009-9163 (Print)
IS  - 0009-9163 (Linking)
VI  - 42
IP  - 2
DP  - 1992 Aug
TI  - A study of ten small supernumerary (marker) chromosomes identified by 
      fluorescence in situ hybridization (FISH).
PG  - 84-90
AB  - In seven cases additional minute chromosomes studied by FISH were identified as 
      no. 3, 11, 15, 18, 21 and X. Findings were unexpected except for partial trisomy 
      21 in an adolescent with minor features of Down's syndrome. Moreover, an i(18p) 
      in a mentally retarded dysmorphic child and an idic(15) in a child with Fallot 
      tetralogy was confirmed. In a child with r(21), a supernumerary marker was shown 
      to be derived from no. 21, while in the mother an additional marker idic(22) was 
      noted.
FAU - Rauch, A
AU  - Rauch A
AD  - Institut fur Humangenetik, Friedrich-Alexander Universitat Erlangen-Nurnberg, 
      FRG.
FAU - Pfeiffer, R A
AU  - Pfeiffer RA
FAU - Trautmann, U
AU  - Trautmann U
FAU - Liehr, T
AU  - Liehr T
FAU - Rott, H D
AU  - Rott HD
FAU - Ulmer, R
AU  - Ulmer R
LA  - eng
PT  - Case Reports
PT  - Journal Article
PL  - Denmark
TA  - Clin Genet
JT  - Clinical genetics
JID - 0253664
RN  - 0 (Genetic Markers)
SB  - IM
MH  - Amniocentesis
MH  - *Chromosome Aberrations
MH  - Chromosomes, Human, Pair 11
MH  - Chromosomes, Human, Pair 15
MH  - Chromosomes, Human, Pair 18
MH  - Chromosomes, Human, Pair 21
MH  - Chromosomes, Human, Pair 3
MH  - Down Syndrome/genetics
MH  - Facial Bones/abnormalities
MH  - Female
MH  - Genetic Markers
MH  - Humans
MH  - In Situ Hybridization
MH  - Infant
MH  - Infant, Newborn
MH  - Intellectual Disability/genetics
MH  - Male
MH  - Microscopy, Fluorescence
MH  - Mosaicism
MH  - Pregnancy
MH  - Skull/abnormalities
MH  - Tetralogy of Fallot/genetics
MH  - *X Chromosome
EDAT- 1992/08/01 00:00
MHDA- 1992/08/01 00:01
CRDT- 1992/08/01 00:00
PHST- 1992/08/01 00:00 [pubmed]
PHST- 1992/08/01 00:01 [medline]
PHST- 1992/08/01 00:00 [entrez]
AID - 10.1111/j.1399-0004.1992.tb03145.x [doi]
PST - ppublish
SO  - Clin Genet. 1992 Aug;42(2):84-90. doi: 10.1111/j.1399-0004.1992.tb03145.x.