Heba Y El Khashab
Overview
Explore the profile of Heba Y El Khashab including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
14
Citations
480
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
11.
Salih M, Seidahmed M, El Khashab H, Hamad M, Bosley T, Burn S, et al.
Tremor Other Hyperkinet Mov (N Y)
. 2015 Jul;
5:306.
PMID: 26203402
Background: The etiology of many cases of childhood-onset chorea remains undetermined, although advances in genomics are revealing both new disease-associated genes and variant phenotypes associated with known genes. Methods: We...
12.
AlAzami A, Patel N, Shamseldin H, Anazi S, Al-Dosari M, Alzahrani F, et al.
Cell Rep
. 2015 Jan;
10(2):148-61.
PMID: 25558065
Our knowledge of disease genes in neurological disorders is incomplete. With the aim of closing this gap, we performed whole-exome sequencing on 143 multiplex consanguineous families in whom known disease...
13.
Al-Qattan S, Wakil S, Anazi S, AlAzami A, Patel N, Shaheen R, et al.
Genet Med
. 2014 Dec;
17(9):719-25.
PMID: 25503496
Purpose: Molecular karyotyping has rapidly become the test of choice in patients with neurocognitive phenotypes, but studies of its clinical utility have largely been limited to outbred populations. In consanguineous...
14.
Salih M, Tzschach A, Oystreck D, Hassan H, AlDrees A, Elmalik S, et al.
Am J Med Genet A
. 2013 May;
161A(6):1207-13.
PMID: 23633300
Genetic factors represent an important etiologic group in the causation of intellectual disability. We describe a Saudi Arabian family with closley related parents in which four of six children were...