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Oscar Diaz-Horta Selected Research

Pierre Robin syndrome with fetal chondrodysplasia

8/2015Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53.

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Oscar Diaz-Horta Research Topics

Disease

4Deafness (Deaf Mutism)
11/2018 - 09/2014
3Type 1 Diabetes Mellitus (Autoimmune Diabetes)
11/2010 - 11/2002
2Sensorineural Hearing Loss
01/2019 - 11/2012
1Pierre Robin syndrome with fetal chondrodysplasia
08/2015
1Megaepiphyseal dwarfism
08/2015
1type 3 Stickler syndrome
08/2015
1KBG syndrome
02/2015
1Diabetic Ketoacidosis (Ketoacidosis, Diabetic)
11/2007

Drug/Important Bio-Agent (IBA)

4Proteins (Proteins, Gene)FDA Link
01/2019 - 11/2012
2AutoantibodiesIBA
11/2007 - 11/2002
1Receptor Tyrosine Kinase-like Orphan ReceptorsIBA
05/2016
1Collagen Type XIIBA
08/2015
1DNA (Deoxyribonucleic Acid)IBA
03/2015
1NucleotidesIBA
09/2014
1MorpholinosIBA
11/2012
1HLA-DR Antigens (HLA-DR)IBA
11/2010
1RNA (Ribonucleic Acid)IBA
11/2007
1Glyburide (Glibenclamide)FDA LinkGeneric
11/2002