PMID- 18428311
OWN - NLM
STAT- MEDLINE
DCOM- 20080523
LR  - 20161021
IS  - 1934-8258 (Electronic)
IS  - 1934-8258 (Linking)
VI  - Chapter 8
DP  - 2001 May
TI  - Diagnosis of microdeletion syndromes by fluorescence in situ hybridization 
      (FISH).
PG  - Unit 8.10
LID - 10.1002/0471142905.hg0810s14 [doi]
AB  - This unit opens with an overview of microdeletions and methods for their 
      detection. It goes on to describe a vast array of autosomal microdeletion 
      syndromes, X-linked microdeletion syndromes, and microduplication syndromes. The 
      final portion of the unit offers guidance for detecting such syndromes with 
      Fluorescence in situ Hybridization (FISH).
FAU - Shaffer, L G
AU  - Shaffer LG
AD  - Baylor College of Medicine, Houston, Texas, USA.
LA  - eng
PT  - Journal Article
PT  - Review
PL  - United States
TA  - Curr Protoc Hum Genet
JT  - Current protocols in human genetics
JID - 101287858
SB  - IM
MH  - Chromosome Aberrations
MH  - *Chromosome Deletion
MH  - Chromosome Disorders/*diagnosis/*genetics
MH  - Female
MH  - Genetic Diseases, X-Linked/diagnosis/genetics
MH  - Genetics, Medical
MH  - Humans
MH  - In Situ Hybridization, Fluorescence/*methods
MH  - Male
MH  - Syndrome
RF  - 86
EDAT- 2008/04/23 09:00
MHDA- 2008/05/24 09:00
CRDT- 2008/04/23 09:00
PHST- 2008/04/23 09:00 [pubmed]
PHST- 2008/05/24 09:00 [medline]
PHST- 2008/04/23 09:00 [entrez]
AID - 10.1002/0471142905.hg0810s14 [doi]
PST - ppublish
SO  - Curr Protoc Hum Genet. 2001 May;Chapter 8:Unit 8.10. doi: 
      10.1002/0471142905.hg0810s14.