Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

588 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Bi-allelic variants in WNT7B disrupt the development of multiple organs in humans.
Bouasker S, Patel N, Greenlees R, Wellesley D, Fares Taie L, Almontashiri NA, Baptista J, Alghamdi MA, Boissel S, Martinovic J, Prokudin I, Holden S, Mudhar HS, Riley LG, Nassif C, Attie-Bitach T, Miguet M, Delous M, Ernest S, Plaisancié J, Calvas P, Rozet JM, Khan AO, Hamdan FF, Jamieson RV, Alkuraya FS, Michaud JL, Chassaing N. Bouasker S, et al. Among authors: alkuraya fs. J Med Genet. 2023 Mar;60(3):294-300. doi: 10.1136/jmedgenet-2022-108475. Epub 2022 Jul 5. J Med Genet. 2023. PMID: 35790350
Characterization of CTNS mutations in Arab patients with cystinosis.
Aldahmesh MA, Humeidan A, Almojalli HA, Khan AO, Rajab M, AL-Abbad AA, Meyer BF, Alkuraya FS. Aldahmesh MA, et al. Among authors: alkuraya fs. Ophthalmic Genet. 2009 Dec;30(4):185-9. doi: 10.3109/13816810903200953. Ophthalmic Genet. 2009. PMID: 19852576
Corneal decompensation in recessive cornea plana.
Khan AO, Aldahmesh MA, Al-Gehedan S, Meyer BF, Alkuraya FS. Khan AO, et al. Among authors: alkuraya fs. Ophthalmic Genet. 2009 Sep;30(3):142-5. doi: 10.1080/13816810902937084. Ophthalmic Genet. 2009. PMID: 19941419
588 results