Sonic hedgehog mutation analysis in patients with VACTERL association

American Journal of Medical Genetics, Part A

Volumn 152, Issue 3, 2010, Pages 781-783

  Aguinaga, Mónica ^a   Zenteno, Juan Carlos ^b   Pérez Cano, Héctor ^b   Morán, Verónica ^c  

^a INSTITUTO NACIONAL DE PERINATOLOGÍA   (Mexico)

^b INSTITUTE OF OPHTHALMOLOGY CONDE DE VALENCIANA   (Mexico)

^c HOSPITAL INFANTIL DE MÉXICO FEDERICO GÓMEZ   (Mexico)

Author keywords

[No Author keywords available]

Indexed keywords

BRCA2 PROTEIN; SONIC HEDGEHOG PROTEIN; TRANSCRIPTION FACTOR GLI3;

ANUS ATRESIA; BONE DEFECT; CONGENITAL HEART MALFORMATION; EMBRYO DEVELOPMENT; ESOPHAGUS ATRESIA; FANCONI ANEMIA; GENE; GENE EXPRESSION; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; HOLOPROSENCEPHALY; HOXD13 GENE; HUMAN; HYDROCEPHALUS; KARYOTYPE; KIDNEY DYSPLASIA; LETTER; LIMB DEFECT; NONHUMAN; OPEN READING FRAME; PALLISTER HALL SYNDROME; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RADIAL DEFECT; SIGNAL TRANSDUCTION; TRACHEOESOPHAGEAL FISTULA; VERTEBRA MALFORMATION;

ABNORMALITIES, MULTIPLE; ANUS, IMPERFORATE; BASE SEQUENCE; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; ESOPHAGEAL ATRESIA; HEART DEFECTS, CONGENITAL; HEDGEHOG PROTEINS; HUMANS; KIDNEY; MUTATION; RADIUS; SPINE; SYNDROME; TRACHEOESOPHAGEAL FISTULA;

ERINACEIDAE;

EID: 77649217211     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33293     Document Type: Letter

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