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Al‐Bakheet, Albandary
61  results:
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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