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Nair, Pratibha
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1

Spectrum of genetic disorders and gene variants in the Unit..:

Bizzari, Sami ; Nair, Pratibha ; Hana, Sayeeda...
Frontiers in Genetics.  14 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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2

Catalogue for Transmission Genetics in Arabs (CTGA) Databas..:

Bizzari, Sami ; Nair, Pratibha ; Deepthi, Asha...
Genes.  12 (2021)  10 - p. 1518 , 2021
Link: https://doi.org/10.3390/..
 
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3

Recessive marfanoid syndrome with herniation associated wit..:

Bizzari, Sami ; El-Bazzal, Lara ; Nair, Pratibha...
European Journal of Medical Genetics.  63 (2020)  5 - p. 103869 , 2020
Link: https://doi.org/10.1016/..
 
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4

Evaluating the Impact of Outpatient Multi-Dose Medication P..:

Nair, Pratibha ; Kee, Kok Wai ; Mah, Choon Siong.
Journal of Primary Care & Community Health.  11 (2020)  - p. 215013272096508 , 2020
Link: https://doi.org/10.1177/..
 
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5

Contribution of next generation sequencing in pediatric pra..:

Nair, Pratibha ; Sabbagh, Sandra ; Mansour, Hicham...
Molecular Genetics & Genomic Medicine.  6 (2018)  6 - p. 1041-1052 , 2018
Link: https://doi.org/10.1002/..
 
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6

Identification of a novel homozygous UNC80 variant in a chi..:

Obeid, Tasneem ; Hamzeh, Abdul Rezzak ; Saif, Fatima...
Metabolic Brain Disease.  33 (2018)  3 - p. 869-873 , 2018
Link: https://doi.org/10.1007/..
 
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7

Novel PDE6A mutation in an Emirati patient with retinitis p..:

Nair, Pratibha ; Hamzeh, AbdulRezzak ; Malik, EtharMustafa...
Oman Journal of Ophthalmology.  10 (2017)  3 - p. 228 , 2017
Link: https://doi.org/10.4103/..
 
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8

Single‐center experience of N‐linked Congenital Disorders o..:

Bastaki, Fatma ; Bizzari, Sami ; Hamici, Sana...
Annals of Human Genetics.  82 (2017)  1 - p. 35-47 , 2017
Link: https://doi.org/10.1111/..
 
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9

Identification of a novel CTCF mutation responsible for syn..:

Bastaki, Fatma ; Nair, Pratibha ; Mohamed, Madiha...
BMC Medical Genetics.  18 (2017)  1 - p. , 2017
Link: https://doi.org/10.1186/..
 
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10

A novel, putatively null, FGD1 variant leading to Aarskog-S..:

Hamzeh, Abdul Rezzak ; Saif, Fatima ; Nair, Pratibha...
BMC Pediatrics.  17 (2017)  1 - p. , 2017
Link: https://doi.org/10.1186/..
 
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11

A Novel Variant in the Endothelin-Converting Enzyme-Like 1 ..:

Hamzeh, Abdul Rezzak ; Nair, Pratibha ; Mohamed, Madiha...
Medical Principles and Practice.  26 (2017)  2 - p. 195-198 , 2017
Link: https://doi.org/10.1159/..
 
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12

Summary of mutations underlying autosomal recessive congeni..:

Bastaki, Fatma ; Mohamed, Madiha ; Nair, Pratibha...
International Journal of Dermatology.  56 (2017)  5 - p. 514-523 , 2017
Link: https://doi.org/10.1111/..
 
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13

Characterization of an Emirati TMEM138 mutation leading to ..:

Bizzari, Sami ; Hamzeh, Abdul Rezzak ; Nair, Pratibha..
Pediatrics International.  59 (2017)  1 - p. 113-114 , 2017
Link: https://doi.org/10.1111/..
 
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14

Meta-analyses of the association of HLA-DRB1 alleles with r..:

Bizzari, Sami ; Nair, Pratibha ; Al Ali, Mahmoud Taleb.
International Journal of Rheumatic Diseases.  20 (2016)  7 - p. 832-838 , 2016
Link: https://doi.org/10.1111/..
 
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15

A novel SOX18 mutation uncovered in Jordanian patient with ..:

Bastaki, Fatma ; Mohamed, Madiha ; Nair, Pratibha...
Molecular and Cellular Probes.  30 (2016)  1 - p. 18-21 , 2016
Link: https://doi.org/10.1016/..
 
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