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Joseph Foster 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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Joseph Foster Research Topics

Disease

3Deafness (Deaf Mutism)
05/2016 - 09/2014
1Branchio-Oto-Renal Syndrome (Branchio Oculo Facial Syndrome)
07/2017
1type 3 Stickler syndrome
08/2015
1Megaepiphyseal dwarfism
08/2015
1Pierre Robin syndrome with fetal chondrodysplasia
08/2015
1KBG syndrome
02/2015
1Hearing Loss (Hearing Impairment)
11/2014
1Polyarteritis Nodosa (Periarteritis Nodosa)
06/2014
1Inflammation (Inflammations)
06/2014
1deficiency of adenosine deaminase 2
06/2014
1Intellectual Disability (Idiocy)
01/2013

Drug/Important Bio-Agent (IBA)

2DNA (Deoxyribonucleic Acid)IBA
07/2017 - 01/2016
1Receptor Tyrosine Kinase-like Orphan ReceptorsIBA
05/2016
1Collagen Type XIIBA
08/2015
1Proteins (Proteins, Gene)FDA Link
02/2015
1Mitochondrial DNA (mtDNA)IBA
11/2014
1NucleotidesIBA
09/2014
1Adenosine DeaminaseIBA
06/2014
1Amino AcidsFDA Link
01/2013