Zoom-in comparative genomic hybridisation arrays for the characterisation of variable breakpoint contiguous gene syndromes.

Journal of medical genetics

Volumn 44, Issue 1, 2007, Pages

  Johnston, Jennifer J ^a   Walker, Robert L ^a   Davis, Sean ^a   Facio, Flavia ^a   Turner, Joyce T ^a   Bick, David P ^a   Daentl, Donna L ^a   Ellison, Jay W ^a   Meltzer, Paul S ^a   Biesecker, Leslie G ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

GLI3 PROTEIN, HUMAN; KRUPPEL LIKE FACTOR; NERVE PROTEIN; UNCLASSIFIED DRUG;

ADOLESCENT; CHILD; CHROMOSOME ANALYSIS; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CRANIOFACIAL MALFORMATION; DNA MICROARRAY; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HUMAN; INFANT; LETTER; METHODOLOGY; MULTIPLE MALFORMATION SYNDROME; NUCLEIC ACID HYBRIDIZATION; SYNDACTYLY; SYNDROME;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHILD; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CRANIOFACIAL ABNORMALITIES; CYTOGENETIC ANALYSIS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KRUPPEL-LIKE TRANSCRIPTION FACTORS; NERVE TISSUE PROTEINS; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; SYNDACTYLY; SYNDROME;

MLCS; MLOWN;

EID: 33846908822     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2006.042473     Document Type: Letter

References (0)