Clinical, genetic, and molecular aspects of split-hand/foot malformation: An update

American Journal of Medical Genetics, Part A

Volumn 161, Issue 11, 2013, Pages 2860-2872

  Gurrieri, Fiorella ^a   Everman, David B ^b  

^a CATHOLIC UNIVERSITY   (Italy)

^b GREENWOOD GENETIC CENTER   (United States)

Author keywords

Congenital limb malformation; Ectrodactyly; SHFM; Split foot; Split hand

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CDH3 GENE; CHROMOSOME 10Q; CHROMOSOME 17P; CHROMOSOME 19P; CHROMOSOME 1Q; CHROMOSOME 2Q; CHROMOSOME 4Q; CHROMOSOME 6Q; CHROMOSOME 7Q; CHROMOSOME INVERSION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CLINICAL ASSESSMENT; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; DISEASE COURSE; DISEASE SEVERITY; DLX5 GENE; ECTRODACTYLY; EEC1 GENE; EEC2 GENE; EEC3 GENE; EEM SYNDROME GENE; GENE; GENE DUPLICATION; GENE INTERACTION; GENE MUTATION; GENETIC DISORDER; GENETIC HETEROGENEITY; GENETIC SCREENING; GENETIC VARIABILITY; HUMAN; MOLECULAR GENETICS; MOLECULAR PATHOLOGY; PATIENT CARE PLANNING; PENETRANCE; PRIORITY JOURNAL; RARE DISEASE; RECURRENT DISEASE; RISK ASSESSMENT; SHFLD1 GENE; SHFLD2 GENE; SHFM1 GENE; SHFM2 GENE; SHFM3 GENE; SHFM4 GENE; SHFM6 GENE; TP63 GENE; WNT10B GENE;

CONGENITAL LIMB MALFORMATION; ECTRODACTYLY; SHFM; SPLIT FOOT; SPLIT HAND;

CHROMOSOME ABERRATIONS; FOOT DEFORMITIES, CONGENITAL; HAND DEFORMITIES, CONGENITAL; HUMANS; MUTATION; PHENOTYPE; QUANTITATIVE TRAIT LOCI; SYNDROME;

EID: 84886235462     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36239     Document Type: Article

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