Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genes

Genomics

Volumn 85, Issue 5, 2005, Pages 608-621

  Kamnasaran, Deepak ^a   Chen, Chih Ping ^b   Devriendt, Koenraad ^c   Mehta, Lakshmi ^d   Cox, Diane W ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

^b MACKAY MEMORIAL HOSPITAL   (Taiwan)

^c University Hospital   (Belgium)

^d SCHNEIDER CHILDREN'S HOSPITAL   (United States)

Author keywords

Brain; Craniofacial; Disease genes; Midline defect

Indexed keywords

ANIMAL TISSUE; ARTICLE; CHROMOSOME 14Q; CHROMOSOME DELETION; CHROMOSOME WALKING; CYTOGENETICS; EMBRYO; FEMALE; GENE DELETION; GENE EXPRESSION; GENE IDENTIFICATION; GENE LOCUS; GENE MAPPING; GENE STRUCTURE; HOLOPROSENCEPHALY; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; ORTHOLOGY; PRIORITY JOURNAL; PROTEIN LOCALIZATION;

ANIMALIA; MURINAE;

EID: 16244411997     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ygeno.2005.01.010     Document Type: Article

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