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Aldahmesh, Mohammed A.
35
results:
Format
Online (35)
Mediatypes
Articles (Online) (21)
OpenAccess-fulltext (14)
Sorted by: Relevance
Sorted by: Year
?
1
Congenital glaucoma and CYP1B1: an old story revisited:
Alsaif, Hessa S.
;
Khan, Arif O.
;
Patel, Nisha
...
Human Genetics. 138 (2018) 8-9 - p. 1043-1049 , 2018
Link:
https://doi.org/10.1007/..
?
2
Expanding the clinical, allelic, and locus heterogeneity of..:
Patel, Nisha
;
Aldahmesh, Mohammed A.
;
Alkuraya, Hisham
...
Genetics in Medicine. 18 (2016) 6 - p. 554-562 , 2016
Link:
https://doi.org/10.1038/..
?
3
Congenital hereditary endothelial dystrophy, not glaucoma, ..:
Khan, Arif O.
;
Aldahmesh, Mohammed A.
;
Alkuraya, Fowzan
Journal of American Association for Pediatric Ophthalmology and Strabismus. 20 (2016) 4 - p. 370-372 , 2016
Link:
https://doi.org/10.1016/..
?
4
Novel phenotypes and loci identified through clinical genom..:
Patel, Nisha
;
Anand, Deepti
;
Monies, Dorota
...
Human Genetics. 136 (2016) 2 - p. 205-225 , 2016
Link:
https://doi.org/10.1007/..
?
5
Characterizing the morbid genome of ciliopathies:
Ciliopathy WorkingGroup
;
Shaheen, Ranad
;
Szymanska, Katarzyna
...
Genome Biology. 17 (2016) 1 - p. , 2016
Link:
https://doi.org/10.1186/..
?
6
Accelerating Novel Candidate Gene Discovery in Neurogenetic..:
Alazami, Anas M.
;
Patel, Nisha
;
Shamseldin, Hanan E.
...
Cell Reports. 10 (2015) 2 - p. 148-161 , 2015
Link:
https://doi.org/10.1016/..
?
7
Exome-based case–control association study using extreme ph..:
Shtir, Corina
;
Aldahmesh, Mohammed A.
;
Al-Dahmash, Saad
...
Human Genetics. 135 (2015) 2 - p. 193-200 , 2015
Link:
https://doi.org/10.1007/..
?
8
Congenital glaucoma with acquired peripheral circumferentia..:
Khan, Arif O.
;
Aldahmesh, Mohammed A.
;
Mohamed, Jawahir Y.
.
Journal of American Association for Pediatric Ophthalmology and Strabismus. 17 (2013) 1 - p. 105-107 , 2013
Link:
https://doi.org/10.1016/..
?
9
Corneal enlargement without optic disk cupping in children ..:
Khan, Arif O.
;
Aldahmesh, Mohammed A.
;
Mohamed, Jawahir Y.
.
Journal of American Association for Pediatric Ophthalmology and Strabismus. 17 (2013) 6 - p. 643-645 , 2013
Link:
https://doi.org/10.1016/..
?
10
Lenticular changes in cerebrotendinous xanthomatosis, a tre..:
Khan, Arif O.
;
Aldahmesh, Mohammed A.
;
Jawaher, Arif
..
Journal of American Association for Pediatric Ophthalmology and Strabismus. 17 (2013) 1 - p. e18 , 2013
Link:
https://doi.org/10.1016/..
?
11
Biometric and Molecular Characterization of Clinically Diag..:
Nowilaty, Sawsan R.
;
Khan, Arif O.
;
Aldahmesh, Mohammed A.
...
American Journal of Ophthalmology. 155 (2013) 2 - p. 361-372.e7 , 2013
Link:
https://doi.org/10.1016/..
?
12
Mutations in LRPAP1 Are Associated with Severe Myopia in Hu..:
Aldahmesh, Mohammed A.
;
Khan, Arif O.
;
Alkuraya, Hisham
...
The American Journal of Human Genetics. 93 (2013) 2 - p. 313-320 , 2013
Link:
https://doi.org/10.1016/..
?
13
Autozygome maps dispensable DNA and reveals potential selec..:
Khalak, Hanif G.
;
Wakil, Salma M.
;
Imtiaz, Faiqa
...
Genetics in Medicine. 14 (2012) 5 - p. 515-519 , 2012
Link:
https://doi.org/10.1038/..
?
14
Homozygous null mutation in ODZ3 causes microphthalmia in h..:
Aldahmesh, Mohammed A.
;
Mohammed, Jawahir Y.
;
Al-Hazzaa, Selwa
.
Genetics in Medicine. 14 (2012) 11 - p. 900-904 , 2012
Link:
https://doi.org/10.1038/..
?
15
Phenotype–genotype correlation in clinically diagnosed rece..:
Khan, Arif O.
;
Aldahmesh, Mohammed A.
;
Meyer, Brian F.
.
Journal of American Association for Pediatric Ophthalmology and Strabismus. 16 (2012) 1 - p. e21 , 2012
Link:
https://doi.org/10.1016/..
1-15