Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome

Clinical Genetics

Volumn 60, Issue 6, 2001, Pages 447-451

  Takahashi, T ^a   Takahashi, I ^a   Komatsu, M ^a   Sawaishi, Y ^a   Higashi, K ^b   Nishimura, G ^c   Saito, H ^a   Takada, G ^a  

^a AKITA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b Fujiwara Memorial Hospital   (Japan)

^c Nasu Chuou Hospital   (Japan)

Author keywords

Multiple synostosis; Noggin gene; Proximal symphalangism

Indexed keywords

NOGGIN;

ANKYLOSIS; ARTHRODESIS; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BONE DISEASE; CARPAL BONE; CASE REPORT; CHILD; CONDUCTION DEAFNESS; CONTROLLED STUDY; FAMILIAL DISEASE; FEMALE; FRAMESHIFT MUTATION; GENE MUTATION; GENETIC ANALYSIS; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOSITY; HUMAN; JAPAN; MALE; MORPHOGENESIS; PRIORITY JOURNAL; PROXIMAL INTERPHALANGEAL JOINT; SYMPTOMATOLOGY; SYNOSTOSIS; TARSAL BONE;

ABNORMALITIES, MULTIPLE; ANKYLOSIS; BONE MORPHOGENETIC PROTEINS; CARRIER PROTEINS; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; FACIES; FEMALE; FINGERS; HEARING LOSS, CONDUCTIVE; HUMANS; MALE; MUTATION; PEDIGREE; PROTEINS; SYNDROME; SYNOSTOSIS; TOES;

EID: 0035695346     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2001.600607.x     Document Type: Article

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4. Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton
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8. Follistatin and noggin are excluded from the zebrafish organizer
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