(Q28215633)

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Identical mutations in NOG can cause either tarsal/carpal coalition syndrome or proximal symphalangism

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Identical mutations in NOG can cause either tarsal/carpal coalition syndrome or proximal symphalangism (English)

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main subject

proximal symphalangism

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M E Dixon

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P Armstrong

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D B Stevens

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M Bamshad

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language of work or name

English

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publication date

2001

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349-53

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cites work

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Strategies for multilocus linkage analysis in humans

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Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis

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Localization of a multiple synostoses-syndrome disease gene to chromosome 17q21-22.

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Localization of the gene (SYM1) for proximal symphalangism to human chromosome 17q21-q22

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Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein

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Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22

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Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21.

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Conductive deafness, symphalangism, and facial abnormalities: the WL syndrome in a Japanese family

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Noggin-mediated antagonism of BMP signaling is required for growth and patterning of the neural tube and somite

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The Spemann organizer signal noggin binds and inactivates bone morphogenetic protein 4

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Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton

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