Delineation of the interstitial 6q25 microdeletion syndrome: refinement of the critical causative region.

American journal of medical genetics. Part A

Volumn 158 A, Issue 6, 2012, Pages 1395-1399

  Michelson, Marina ^a   Ben Sasson, Anat ^b   Vinkler, Chana ^b   Leshinsky Silver, Esther ^b   Netzer, Ifat ^b   Frumkin, Ayala ^b   Kivity, Sara ^b   Lerman Sagie, Tally ^b   Lev, Dorit ^b  

^a Wolfson Medical Center   (Israel)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAIN; CASE REPORT; CHROMOSOME 6; CHROMOSOME DELETION; COMPARATIVE GENOMIC HYBRIDIZATION; FACIES; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HUMAN; INFANT; MALE; MULTIPLE MALFORMATION SYNDROME; PATHOLOGY; SYNDROME;

ABNORMALITIES, MULTIPLE; BRAIN; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 6; COMPARATIVE GENOMIC HYBRIDIZATION; FACIES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; SYNDROME;

MLCS; MLOWN;

EID: 85027947495     PISSN: None     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.35361     Document Type: Article

References (0)