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Shahid M Baig Selected Research

Grebe type Chondrodysplasia

7/2021A GDF5 frameshift mutation segregating with Grebe type chondrodysplasia and brachydactyly type C+ in a 6 generations family: Clinical report and mini review.

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Shahid M Baig Research Topics

Disease

1Hearing Loss (Hearing Impairment)
12/2021
1Primary Ovarian Insufficiency
12/2021
1Seizures (Absence Seizure)
12/2021
1Intellectual Disability (Idiocy)
12/2021
1Grebe type Chondrodysplasia
07/2021
1Brachydactyly type C
07/2021
1Diamond-Blackfan Anemia (Anemia, Diamond Blackfan)
12/2020
1Neurodevelopmental Disorders
11/2019
1Neurocognitive Disorders (Clerambault Syndrome)
11/2019
1Microcephaly
01/2019
1Infections
01/2018
1Hypohidrosis
07/2017
1Renal Insufficiency (Renal Failure)
07/2017
1Secondary Hyperparathyroidism
07/2017
1Autosomal Recessive Primary Microcephaly
11/2014
1Autosomal Dominant 48 Deafness
05/2014
1Nonsyndromic Deafness
05/2014
1Inflammation (Inflammations)
04/2013
1Insulin Resistance
04/2013
1Body Weight (Weight, Body)
04/2013
1Obesity
04/2013
1Deafness (Deaf Mutism)
01/2011
1Cardiac Arrhythmias (Arrythmia)
01/2011
1Jervell-Lange Nielsen Syndrome (Jervell and Lange-Nielsen Syndrome)
01/2011

Drug/Important Bio-Agent (IBA)

3Proteins (Proteins, Gene)FDA Link
11/2019 - 01/2018
1Mitochondrial DNA (mtDNA)IBA
12/2021
1Gonadal Steroid Hormones (Sex Hormones)IBA
12/2021
1Growth Differentiation Factor 5IBA
07/2021
1Ribosomal Proteins (Ribosomal Protein)IBA
12/2020
1Transcription Factors (Transcription Factor)IBA
11/2019
1Histones (Histone)IBA
01/2018
1CationsIBA
07/2017
1Centrosomal Associated ProteinsIBA
11/2014
1Nonsense Codon (Nonsense Mutation)IBA
05/2014
1Leukocyte Elastase (Neutrophil Elastase)IBA
04/2013
1GW 311616IBA
04/2013
1Delayed Rectifier Potassium ChannelsIBA
01/2011