The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients

Human Molecular Genetics

Volumn 6, Issue 2, 1997, Pages 247-258

  Wilming, Laurens G ^a   Snoeren, C A Sylvia ^a   Van Rijswijk, Angelique ^a,b   Grosveld, Frank ^b   Meijers, Carel ^a,b  

^a ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

^b ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; HISTONE;

ALTERNATIVE RNA SPLICING; ANIMAL TISSUE; ARTICLE; BIRTH DEFECT; CHROMATIN; CHROMOSOME 22Q; CONGENITAL HEART MALFORMATION; CRANIOFACIAL MALFORMATION; DIGEORGE SYNDROME; EMBRYO; EMBRYO DEVELOPMENT; EMBRYONIC STRUCTURES; ENDODERM; HUMAN; IN SITU HYBRIDIZATION; LIMB BUD; MOUSE; NEURAL CREST; NEURAL CREST CELL; NONHUMAN; PHARYNX; PRIORITY JOURNAL; PROTEIN ASSEMBLY; RHOMBENCEPHALON; SEQUENCE HOMOLOGY; THYMUS DISEASE;

ALTERNATIVE SPLICING; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; BRANCHIAL REGION; CELL CYCLE PROTEINS; CHROMOSOMAL PROTEINS, NON-HISTONE; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 22; CLONING, MOLECULAR; DIGEORGE SYNDROME; DNA, COMPLEMENTARY; DNA-BINDING PROTEINS; EMBRYO; EXONS; FEMALE; GASTRULA; GENE EXPRESSION; HUMANS; LIMB BUD; MALE; MICE; MOLECULAR SEQUENCE DATA; NEURAL CREST; NUCLEAR PROTEINS; SEQUENCE HOMOLOGY, AMINO ACID; TRANSCRIPTION FACTORS;

ANIMALIA; MAMMALIA; MURINAE;

EID: 0031058266     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/6.2.247     Document Type: Article

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