Hesham M Aldhalaan

Hesham M Aldhalaan

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Hesham M Aldhalaan

Hesham M Aldhalaan

Publications by authors named "Hesham M Aldhalaan"

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Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy.

Nat Commun 2020 Jan 30;11(1):595. Epub 2020 Jan 30.

Institute of Medical Biology, A*STAR, Biopolis, Singapore, 138648, Singapore.

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http://dx.doi.org/10.1038/s41467-020-14360-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6992768PMC
January 2020

Services for children with autism in the Kingdom of Saudi Arabia.

Autism 2017 07 20;21(5):592-602. Epub 2016 Oct 20.

1 University of California, Los Angeles, USA.

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http://dx.doi.org/10.1177/1362361316664868DOI Listing
July 2017

The clinical spectrum of homozygous HOXA1 mutations.

Am J Med Genet A 2008 May;146A(10):1235-40

The Neuro-ophthalmology Division, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1002/ajmg.a.32262DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3517166PMC
May 2008