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Nair, Pratibha
114
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Online (114)
Mediatypes
Articles (Online) (61)
Bookchapter (Online) (1)
OpenAccess-fulltext (52)
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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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
1-15