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The American Journal of Human Genetics, ISSN 0002-9297, 12/2015, Volume 97, Issue 6, pp. 848 - 854
Journal Article
PLoS Genetics, ISSN 1553-7390, 03/2016, Volume 12, Issue 3, p. e1005936
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European Journal of Human Genetics, ISSN 1018-4813, 06/2018, Volume 26, Issue 6, pp. 876 - 885
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The American Journal of Human Genetics, ISSN 0002-9297, 10/2012, Volume 91, Issue 4, pp. 629 - 635
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The American Journal of Human Genetics, ISSN 0002-9297, 06/2018, Volume 102, Issue 6, pp. 1115 - 1125
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Clinical Genetics, ISSN 0009-9163, 12/2012, Volume 82, Issue 6, pp. 514 - 520
Usami S, Abe S, Nishio S, Sakurai Y, Kojima H, Tono T, Suzuki N. Mutations in the NOG gene are commonly found in congenital stapes ankylosis with... 
stapes ankylosis with broad | Teunissen and Cremer syndrome | stapes ankylosis | otosclerosis | symphalangism | SYM1 | thumb and toes | Stapes ankylosis | Thumb and toes | Symphalangism | Stapes ankylosis with broad | Otosclerosis | FACIOAUDIOSYMPHALANGISM SYNDROME | CARPAL | TARSAL | FEATURES | CONDUCTIVE HEARING-LOSS | PROXIMAL SYMPHALANGISM | GROWTH | GENETICS & HEREDITY | TEUNISSEN-CREMERS-SYNDROME | MULTIPLE-SYNOSTOSIS SYNDROME | ENCODING NOGGIN | Stapes - abnormalities | Tarsal Bones - abnormalities | Humans | Middle Aged | Asian Continental Ancestry Group - genetics | Male | DNA Primers - genetics | Syndactyly - pathology | Ankylosis - genetics | Hyperopia - genetics | Thumb - pathology | Polymerase Chain Reaction | Adult | Female | Otosclerosis - genetics | Toes - pathology | Hyperopia - pathology | Ankylosis - pathology | Carpal Bones - abnormalities | Genetic Predisposition to Disease - genetics | Joint Diseases - pathology | Synostosis | Joint Diseases - genetics | Foot Deformities, Congenital | Hearing Loss, Conductive - pathology | Joint Diseases - congenital | Mutation - genetics | Sequence Analysis, DNA | Finger Joint - pathology | Carrier Proteins - genetics | Hand Deformities, Congenital | Phenotype | Pedigree | Hearing Loss, Conductive - genetics | Aged | Thumb - abnormalities | Toes - abnormalities | Finger Joint - abnormalities | Stapes - pathology | Syndactyly - genetics | Medical colleges | Cysteine | Anopheles | Genetic disorders | Codon | Analysis | Genes | Genetic research | Genetic aspects | Genetic screening | Genotype & phenotype | Ears & hearing | Skeletal system | Congenital diseases | Mutation | Literature reviews | Ankylosis | Surgery | Dysostosis | Noggin protein | Symphalangia | NOG gene | Original
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PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 7, p. e11493
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European Journal of Human Genetics, ISSN 1018-4813, 08/2012, Volume 20, Issue 8, pp. 817 - 824
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Human Molecular Genetics, ISSN 0964-6906, 04/2017, Volume 26, Issue 7, pp. 1280 - 1293
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Nature Reviews Endocrinology, ISSN 1759-5029, 04/2016, Volume 12, Issue 4, pp. 203 - 221
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