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COL11A2
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#	Item
1	Molecular Genetics Service Profile Stickler dysplasia Introduction ◊ ◊ Add to Reading List Source URL: www.esdn.org Language: English - Date: 2009-03-19 12:03:51 Collagen disease Collagen type XI alpha 1 Collagen type II alpha 1 COL11A2 Genetic testing Collagenopathy types II and XI Stickler syndrome Genetics Medicine Health
2	Molecular Genetics Service Profile Otospondylomegaepiphyseal dysplasia (OSMED) Introduction ◊ ◊ Add to Reading List Source URL: www.esdn.org Language: English - Date: 2009-03-19 12:03:51 Rare diseases Biology COL11A2 Syndromes Otospondylomegaepiphyseal dysplasia Weissenbacher–Zweymüller syndrome Mutation Collagen disease Health Genetics
3	Stickler Syndrome Basic Information for Patients and Families Stickler syndrome is a genetic disorder affecting collagen throughout the body. Collagen is a primary part of connective tissue like bone, skin and cartilage. Add to Reading List Source URL: www.sticklers.org Language: English - Date: 2008-04-02 21:41:47 Collagen disease Rare diseases Rheumatology Stickler syndrome COL11A2 Collagen type XI alpha 1 Marshall syndrome Collagen type II alpha 1 Health Syndromes Medicine
4	The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitro Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Philosophy of biology Nonsyndromic deafness Mutation Sensorineural hearing loss Chromosome 11 DIAPH1 COL11A2 Point mutation Congenital hearing loss Deafness Biology Genetics

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