Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome

American Journal of Medical Genetics, Part A

Volumn 143, Issue 22, 2007, Pages 2668-2674

  Abo Dalo, Benjamin ^a   Kim, Hyung Goo ^b,f   Roes, Melanie ^a   Stefanova, Margarita ^a,c   Higgins, Anne ^d   Shen, Yiping ^b   Mundlos, Stefan ^e   Quade, Bradley J ^d   Gusella, James F ^b   Kutsche, Kerstin ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b MASSACHUSETTS GENERAL HOSPITAL   (United States)

^c MEDICAL UNIVERSITY OF PLOVDIV   (Bulgaria)

^d BRIGHAM AND WOMEN S HOSPITAL   (United States)

^e MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

^f MEDICAL COLLEGE OF GEORGIA   (United States)

Author keywords

CACNA2D3; Chromosome translocation; Gingival hyperplasia; WNT5A; Zimmermann Laband syndrome

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 3P; CHROMOSOME MAP; CHROMOSOME TRANSLOCATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENE DISRUPTION; GENE MUTATION; GENETIC ANALYSIS; GENETIC RECOMBINATION; GENETIC SCREENING; HUMAN; HUMAN CELL; KARYOTYPE; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; REGULATORY SEQUENCE; SOUTHERN BLOTTING; ZIMMERMANN LABAND SYNDROME;

ABNORMALITIES, MULTIPLE; CALCIUM CHANNELS; CHROMOSOME ABERRATIONS; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 17; CHROMOSOMES, HUMAN, PAIR 3; CHROMOSOMES, HUMAN, PAIR 8; CRANIOFACIAL ABNORMALITIES; DNA MUTATIONAL ANALYSIS; HUMANS; KARYOTYPING; PROTO-ONCOGENE PROTEINS; SYNDROME; TRANSLOCATION, GENETIC; WNT PROTEINS;

EID: 35948955894     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32034     Document Type: Article

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