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Suhaila Al‐Bahlani
Observed names:
Suhaila Al Bahlani,
Suhaila Al-Bahlani
Institutions:
Ministry of Health,
Al Nahdha Hospital
Observed institutions:
Ministry of Health,
Al Nahdha Hospital
OpenAlex ID:
A5110071625
Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta
2009
·
Walid El-Sayed
, David A. Parry
, et al.
·
The American Journal of Human Genetics
·
161
Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations
2013
·
Graciana Jaureguiberry
, Muriel De la Dure-Molla
, et al.
·
Nephron Physiology
·
105
PDF
Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta
2012
·
David A. Parry
, Steven J. Brookes
, et al.
·
The American Journal of Human Genetics
·
100
PDF
Spectrum of pathogenic variants and founder effects in amelogenesis imperfecta associated with MMP20
2021
·
Georgios Nikolopoulos
, Claire E. L. Smith
, et al.
·
Human Mutation
·
9
PDF
Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability
2024
·
Claire E L Smith
, Virginie Laugel-Haushalter
, et al.
·
Journal of Medical Genetics
·
6
Front & Back Matter
2012
·
Namhee Kim
, Surinder Cheema-Dhadli
, et al.
·
Nephron Physiology
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Works count:
6
Citation count:
381
H-index:
5
I10-index:
3
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