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Imen Chakchouk 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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Imen Chakchouk Research Topics

Disease

3Hearing Loss (Hearing Impairment)
08/2021 - 05/2016
2Deafness (Deaf Mutism)
05/2016 - 05/2015
1Autosomal Recessive 30 Deafness
08/2021
1Hydatidiform Mole (Molar Pregnancy)
01/2021
1Intellectual Disability (Idiocy)
09/2018
1Microcephaly
09/2018
1Megaepiphyseal dwarfism
08/2015
1Pierre Robin syndrome with fetal chondrodysplasia
08/2015
1type 3 Stickler syndrome
08/2015
1Autosomal Recessive 66 Deafness
05/2015

Drug/Important Bio-Agent (IBA)

3Proteins (Proteins, Gene)FDA Link
01/2021 - 05/2015
2DNA (Deoxyribonucleic Acid)IBA
09/2018 - 05/2016
1Phosphotransferases (Kinase)IBA
08/2021
1CationsIBA
05/2016
1Protein Isoforms (Isoforms)IBA
05/2016
1Collagen Type XIIBA
08/2015