Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development

Human Molecular Genetics

Volumn 5, Issue 5, 1996, Pages 571-579

  Crackower, Michael A ^a,b   Scherer, Stephen W ^b   Rommens, Johanna M ^a,b   Hui, Chi Chung ^a,b   Poorkaj, Parvoneh ^c   Soder, Sylvia ^b   Cobben, Jan Maarten ^d   Hudgins, Louanne ^e   Evans, James P ^f   Tsui, Lap Chee ^a,b  

^a UNIVERSITY OF TORONTO   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c UNIVERSITY OF WASHINGTON   (United States)

^d UNIVERSITY OF GRONINGEN   (Netherlands)

^e SEATTLE CHILDREN S RESEARCH INSTITUTE   (United States)

^f UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

POLYPEPTIDE;

ANIMAL TISSUE; ARTICLE; CHROMOSOME 7Q; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; EMBRYO; FINGER MALFORMATION; FOOT MALFORMATION; GENE LOCUS; HAND MALFORMATION; HOMEOBOX; HUMAN; HUMAN CELL; INTERSTITIAL CHROMOSOME DELETION; LIMB DEVELOPMENT; MULTIGENE FAMILY; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; RNA HYBRIDIZATION; SEQUENCE HOMOLOGY; TISSUE SPECIFICITY; YEAST ARTIFICIAL CHROMOSOME;

AMINO ACID SEQUENCE; BASE SEQUENCE; BLOTTING, NORTHERN; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 7; COSMIDS; FOOT DEFORMITIES, CONGENITAL; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENES, HOMEOBOX; HAND DEFORMITIES, CONGENITAL; HOMEODOMAIN PROTEINS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; MOLECULAR SEQUENCE DATA; SEQUENCE HOMOLOGY, AMINO ACID; SEQUENCE HOMOLOGY, NUCLEIC ACID; TRANSCRIPTION FACTORS;

EID: 9244248158     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.5.571     Document Type: Article

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