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Aldahmesh, Mohammed A.
14
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1
Infantile Nephropathic Cystinosis: A Novel CTNS Mutation:
Aldahmesh, Mohammed
;
Döneray, Hakan
;
Orbak, Zerrin
..
cd558bbd-5471-478c-bfd3-da72e461041c. , 2017
Link:
https://doi.org/10.5152/..
?
2
Infantile Nephropathic Cystinosis: A Novel CTNS Mutation:
Doneray, Hakan
;
Aldahmesh, Mohammed
;
Yilmaz, Gulsah
..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5469843/. , 2017
Link:
http://www.ncbi.nlm.nih...
?
3
Characterizing the morbid genome of ciliopathies:
Shaheen, Ranad
;
Szymanska, Katarzyna
;
Basu, Basudha
...
http://genomebiology.com/2016/17/1/242. , 2016
Link:
http://genomebiology.com..
?
4
Novel phenotypes and loci identified through clinical genom..:
Patel, Nisha
;
Anand, Deepti
;
Monies, Dorota
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783298/. , 2016
Link:
http://www.ncbi.nlm.nih...
?
5
Phenotypes of Recessive Pediatric Cataract in a Cohort of C..:
Khan, Arif O
;
Aldahmesh, Mohammed A
;
Alkuraya, Fowzan S
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4634221/. , 2015
Link:
http://www.ncbi.nlm.nih...
?
6
An siRNA-based functional genomics screen for the identific..:
Wheway, Gabrielle
;
Schmidts, Miriam
;
Mans, Dorus A
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4536769/. , 2015
Link:
http://www.ncbi.nlm.nih...
?
7
Mutations in LRPAP1 Are Associated with Severe Myopia in Hu..:
Aldahmesh, Mohammed A
;
Khan, Arif O
;
Alkuraya, Hisham
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738831. , 2013
Link:
http://www.ncbi.nlm.nih...
?
8
Mutations in C12orf57 Cause a Syndromic Form of Colobomatou..:
Zahrani, Fatema
;
Aldahmesh, Mohammed A
;
Alshammari, Muneera J
..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591839. , 2013
Link:
http://www.ncbi.nlm.nih...
?
9
Recessive Mutations in ELOVL4 Cause Ichthyosis, Intellectua..:
Aldahmesh, Mohammed A
;
Mohamed, Jawahir Y
;
Alkuraya, Hisham S
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234380. , 2011
Link:
http://www.ncbi.nlm.nih...
?
10
Novel mutations in MERTK associated with childhood onset ro..:
Mackay, Donna S
;
Henderson, Robert H
;
Sergouniotis, Panagiotis I
...
qt0037f4t1. , 2010
Link:
https://escholarship.org..
?
11
MeltMADGE for mutation scanning of specific genes in popula..:
Alharbi, Khalid K
;
Aldahmesh, Mohammed A
;
Gaunt, Tom R
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3575632. , 2010
Link:
http://www.ncbi.nlm.nih...
?
12
The enhanced S‐cone syndrome in children:
Khan, Arif O
;
Aldahmesh, Mohammed
;
Meyer, Brian
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1857689. , 2007
Link:
http://www.ncbi.nlm.nih...
?
13
Mutation scanning by meltMADGE: Validations using BRCA1 and..:
Alharbi, Khalid K
;
Aldahmesh, Mohammed A
;
Spanakis, Emmanuel
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1172041. , 2005
Link:
http://www.ncbi.nlm.nih...
?
14
Accelerating Novel Candidate Gene Discovery in Neurogenetic..:
Anas M. Alazami
;
Nisha Patel
;
Hanan E. Shamseldin
...
http://www.sciencedirect.com/science/article/pii/S2211124714010444. , 2015
Link:
https://doi.org/10.1016/..
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