Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects

Nature Genetics

Volumn 27, Issue 1, 2001, Pages 17-18

  Mavrogiannis, Lampros A ^a   Antonopoulou, Ileana ^b   Baxová, Alica ^c   Kutílek, Stepán ^c   Kim, Chong A ^d   Sugayama, Sofia M ^d   Salamanca, Alberto ^e   Wall, Steven A ^f   Morriss Kay, Gillian M ^b   Wilkie, Andrew O M ^a,f,g  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b UNIVERSITY OF OXFORD   (United Kingdom)

^c CHARLES UNIVERSITY   (Czech Republic)

^d UNIVERSITY OF SÃO PAULO   (Brazil)

^e UNIVERSITY OF GRANADA   (Spain)

^f RADCLIFFE INFIRMARY   (United Kingdom)

^g The Churchill ^*  (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

AMINO ACID SEQUENCE; ANIMAL CELL; ANIMAL MODEL; ARTICLE; BONE DEFECT; CRANIOFACIAL SYNOSTOSIS; DNA BINDING; EMBRYO; GENE MAPPING; GENE MUTATION; GENETIC LINKAGE; GENETIC TRANSCRIPTION; HOMEOBOX; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; OSSIFICATION; OSTEOBLAST; PHENOTYPE; PRIORITY JOURNAL; SKULL DEFECT;

ANIMALS; BASE SEQUENCE; CRANIOFACIAL ABNORMALITIES; DNA MUTATIONAL ANALYSIS; DNA-BINDING PROTEINS; EXONS; GENES, HOMEOBOX; HOMEODOMAIN PROTEINS; HUMANS; MICE; MOLECULAR SEQUENCE DATA; MUTATION; OSTEOGENESIS; PHENOTYPE; PHYSICAL CHROMOSOME MAPPING; PROTEINS; SKULL; TRANSCRIPTION FACTORS;

ANIMALIA; MAMMALIA;

EID: 0035158663     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/83703     Document Type: Article

References (15)