|1.||Takeno, Sachio: 1 article (09/2015)|
|2.||Ishino, Takashi: 1 article (09/2015)|
|3.||Hirakawa, Katsuhiro: 1 article (09/2015)|
|4.||Borra, Vere: 1 article (01/2013)|
|5.||Van Hul, Wim: 1 article (01/2013)|
|6.||van den Ende, Jenneke J: 1 article (01/2013)|
|7.||Petty, Elizabeth M: 1 article (08/2011)|
|8.||Potti, Tommy A: 1 article (08/2011)|
|9.||Lesperance, Marci M: 1 article (08/2011)|
|10.||Schmidt, Thorsten: 1 article (06/2010)|
09/01/2005 - "Stapes ankylosis in a family with a novel NOG mutation: otologic features of the facioaudiosymphalangism syndrome."
09/01/2015 - "Human noggin (NOG) gene mutation causes multiple bony disorders showing up as stapes ankylosis with broad thumbs and toes (SABTT), proximal symphalangism (SYM1), multiple synostoses syndrome 1 (SYNS1), tarsal-carpal coalition syndrome (TCC) and brachydactyly type B2 (BDB2). "
08/01/2011 - "These include (1) proximal symphalangism; (2) multiple synostoses syndrome 1; (3) stapes ankylosis with broad thumbs and toes; (4) tarsal-carpal coalition syndrome; and (5) brachydactyly type B2. "
06/01/2010 - "We report on a father and son with facioaudiosymphalangism syndrome, an alternative designation for multiple synostoses syndrome, type I. This syndrome includes synostosis, brachydactyly, craniofacial dysmorphic features, stapes fixation, hyperopia, and growth retardation. "
01/01/2013 - "We report on a patient with a clinical phenotype showing all the features of the multiple synostoses syndrome or the facioaudiosymphalangism syndrome, including symphalangism, condunction deafness, and the typical facies. "
|5.||Deafness (Deaf Mutism)
|1.||Tarsal carpal coalition syndrome