PMID- 20891031
OWN - NLM
STAT- MEDLINE
DCOM- 20110111
LR  - 20161021
IS  - 1934-8258 (Electronic)
IS  - 1934-8258 (Linking)
VI  - Chapter 8
DP  - 2010 Oct
TI  - Diagnosis of cryptic chromosomal syndromes by fluorescence in situ hybridization 
      (FISH).
PG  - Unit 8.10.1-20
LID - 10.1002/0471142905.hg0810s67 [doi]
AB  - This unit describes the various methods by which cytogeneticists detect 
      chromosome abnormalities. The unit offers guidance for detecting such 
      abnormalities with fluorescence in situ hybridization (FISH), as well as the 
      benefits, limitations, and other applications of FISH.
CI  - Curr. Protoc. Hum. Genet. 67:8.10.1-8.10.20 (c) 2010 by John Wiley & Sons, Inc.
FAU - Kashork, Catherine D
AU  - Kashork CD
AD  - Signature Genomic Laboratories, Spokane, Washington, USA.
FAU - Theisen, Aaron
AU  - Theisen A
FAU - Shaffer, Lisa G
AU  - Shaffer LG
LA  - eng
PT  - Journal Article
PL  - United States
TA  - Curr Protoc Hum Genet
JT  - Current protocols in human genetics
JID - 101287858
SB  - IM
MH  - Abnormalities, Multiple/*genetics
MH  - *Chromosome Aberrations
MH  - Cytogenetics
MH  - Genetics, Medical
MH  - Humans
MH  - In Situ Hybridization, Fluorescence/*methods
MH  - Syndrome
EDAT- 2010/10/05 06:00
MHDA- 2011/01/12 06:00
CRDT- 2010/10/05 06:00
PHST- 2010/10/05 06:00 [entrez]
PHST- 2010/10/05 06:00 [pubmed]
PHST- 2011/01/12 06:00 [medline]
AID - 10.1002/0471142905.hg0810s67 [doi]
PST - ppublish
SO  - Curr Protoc Hum Genet. 2010 Oct;Chapter 8:Unit 8.10.1-20. doi: 
      10.1002/0471142905.hg0810s67.