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Al‐Bakheet, Albandary
61
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Online (61)
Mediatypes
Articles (Online) (30)
OpenAccess-fulltext (31)
Sorted by: Relevance
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1
Expanding the phenotypic and genotypic spectrum of GGPS1 re..:
Altassan, Ruqaiah
;
AlQudairy, Hanan
;
AlJebreen, Sarah
...
American Journal of Medical Genetics Part A. 194 (2023) 4 - p. , 2023
Link:
https://doi.org/10.1002/..
?
2
Clinical, radiological, and genetic characterization of SLC..:
AlQudairy, Hanan
;
AlDhalaan, Hesham
;
AlRuways, Sarah
...
Frontiers in Pediatrics. 10 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
3
Detailed genetic and clinical analysis of a novel de novo v..:
AlBakheet, Albandary
;
AlQudairy, Hanan
;
Alkhalifah, Joud
...
Frontiers in Genetics. 13 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
4
A Novel Homozygous Founder Variant of RTN4IP1 in Two Consan..:
Aldosary, Mazhor
;
Alsagob, Maysoon
;
AlQudairy, Hanan
...
Cells. 11 (2022) 19 - p. 3154 , 2022
Link:
https://doi.org/10.3390/..
?
5
Genetic Causes, Clinical Manifestations and Diagnosis of Ce..:
Alomrani, Basmah
;
Javed, Murid
;
Mohammed Ali, Hani S. H.
...
Journal of Contemporary Medical Sciences. 8 (2022) 1 - p. , 2022
Link:
https://doi.org/10.22317..
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6
Global Transcriptional Profiling of Granulosa Cells from Po..:
Daghestani, Maha H.
;
Alqahtani, Huda A.
;
AlBakheet, AlBandary
...
Journal of Clinical Medicine. 11 (2022) 23 - p. 6941 , 2022
Link:
https://doi.org/10.3390/..
?
7
A Novel GEMIN4 Variant in a Consanguineous Family Leads to ..:
Aldhalaan, Hesham
;
AlBakheet, Albandary
;
AlRuways, Sarah
...
Genes. 13 (2021) 1 - p. 92 , 2021
Link:
https://doi.org/10.3390/..
?
8
SLC25A42‐associated mitochondrial encephalomyopathy: Report..:
Aldosary, Mazhor
;
Baselm, Shahad
;
Abdulrahim, Maha
...
JIMD Reports. 60 (2021) 1 - p. 75-87 , 2021
Link:
https://doi.org/10.1002/..
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9
Genetics of ataxia telangiectasia in a highly consanguineou..:
Al‐Muhaizea, Mohammed A.
;
Aldeeb, Hanouf
;
Almass, Rawan
...
Annals of Human Genetics. 86 (2021) 1 - p. 34-44 , 2021
Link:
https://doi.org/10.1111/..
?
10
Hematological findings associated with tubulin‐folding cofa..:
Al‐Bakheet, Albandary
;
Tohary, Mohamed
;
Khan, Sameena
...
Clinical Genetics. 99 (2021) 5 - p. 724-731 , 2021
Link:
https://doi.org/10.1111/..
?
11
Ancient founder mutation in RUBCN: a second unrelated famil..:
Seidahmed, Mohammed Z.
;
Hamad, Muddathir H.
;
AlBakheet, Albandary
...
BMC Neurology. 20 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1186/..
?
12
Pyrostigmine therapy in a patient with VAMP1-related congen..:
Al-Muhaizea, Mohammad A.
;
AlQuait, Laila
;
AlRasheed, Afnan
...
Neuromuscular Disorders. 30 (2020) 7 - p. 611-615 , 2020
Link:
https://doi.org/10.1016/..
?
13
Identification of novel genomic imbalances in Saudi patient..:
Al-Hassnan, Zuhair N.
;
Albawardi, Waad
;
Almutairi, Faten
...
Molecular Cytogenetics. 11 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
?
14
Breast stromal fibroblasts from histologically normal surgi..:
Al‐Rakan, Maha A
;
Colak, Dilek
;
Hendrayani, Siti‐Faujiah
...
The Journal of Pathology. 231 (2013) 4 - p. 457-465 , 2013
Link:
https://doi.org/10.1002/..
?
15
A novel mutation in a large family causes a unique phenotyp..:
AlBakheet, AlBandary
;
Qari, Aliya
;
Colak, Dilek
...
Gene. 526 (2013) 2 - p. 464-466 , 2013
Link:
https://doi.org/10.1016/..
1-15