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Alanzi, Talal
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1

Prenatal Diagnosis of c.437–1G>A Mutation in the MAN2B1 Gen..:

AlAnzi, Talal ; Mohammed, Sarar ; AlHashem, Amal.
Cureus.  , 2024
Link: https://doi.org/10.7759/..
 
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2

Expanding the allelic spectrum of ELOVL4‐related autosomal ..:

Alabdulrazzaq, Fatima ; Alanzi, Talal ; Al‐Balool, Haya H....
Molecular Genetics & Genomic Medicine.  11 (2023)  12 - p. , 2023
Link: https://doi.org/10.1002/..
 
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3

Spectrum of FAR1 (Fatty Acyl‐CoA Reductase 1) Variants and ..:

Westenberger, Ana ; Ruiz‐Herrera, Adriana ; Bozdoğan, Sevcan...
Movement Disorders.  38 (2023)  3 - p. 502-504 , 2023
Link: https://doi.org/10.1002/..
 
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4

Genotype and Phenotype of Adenosine Deaminase 2 Deficiency:..:

Alabbas, Fahad ; Alanzi, Talal ; Alrasheed, Abdulrahman...
Journal of Clinical Immunology.  43 (2022)  2 - p. 338-349 , 2022
Link: https://doi.org/10.1007/..
 
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5

A novel variant of RBCK1 gene causes mild polyglucosan myop..:

AlAnzi, Talal ; Al Harbi, Fahad ; AlGhamdi, AbdulAziz.
Neurosciences.  27 (2022)  1 - p. 45-49 , 2022
Link: https://doi.org/10.17712..
 
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6

The first Saudi baby with classic homocystinuria diagnosed ..:

AlAnzi, Talal ; Al Harbi, Fahad J. ; AlFaifii, Joharah.
Saudi Medical Journal.  42 (2021)  2 - p. 219-222 , 2021
Link: https://doi.org/10.15537..
 
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7

Wolman's disease presenting with secondary hemophagocytic l..:

Alabbas, Fahad ; Elyamany, Ghaleb ; Alanzi, Talal...
BMC Pediatrics.  21 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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8

Proteus syndrome caused by novel somatic AKT1 duplication:

AlAnzi, Talal ; Al-mashharawi, Eman ; Alhashem, Amal
Saudi Medical Journal.  42 (2021)  1 - p. 95-99 , 2021
Link: https://doi.org/10.15537..
 
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9

Development and validation of a score for emergency interve..:

Al-Terki, Abdullatif ; El-Nahas, Ahmed R. ; Abdelhamid, Usama...
Arab Journal of Urology.  18 (2020)  4 - p. 236-240 , 2020
Link: https://doi.org/10.1080/..
 
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10

An exome-first approach to aid in the diagnosis of primary ..:

Shamseldin, Hanan E. ; Al Mogarri, Ibrahim ; Alqwaiee, Mansour M....
Human Genetics.  139 (2020)  10 - p. 1273-1283 , 2020
Link: https://doi.org/10.1007/..
 
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11

A de novo splicing variant supports the candidacy of TLL1 i..:

Alanzi, Talal ; Alhashem, Amal ; Dagriri, Khalid..
European Journal of Human Genetics.  28 (2019)  4 - p. 525-528 , 2019
Link: https://doi.org/10.1038/..
 
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12

Spectrum of bone marrow pathology and hematological abnorma..:

Bakshi, Nasir A. ; Al‐Anzi, Talal ; Mohamed, Said Y....
American Journal of Medical Genetics Part A.  176 (2018)  3 - p. 687-691 , 2018
Link: https://doi.org/10.1002/..
 
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13

Grafted tubularised incised-plate urethroplasty: An objecti..:

Gupta, Vipul ; Yadav, Sunil Kumar ; Alanzi, Talal...
Arab Journal of Urology.  14 (2016)  4 - p. 299-304 , 2016
Link: https://doi.org/10.1016/..
 
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14

A homozygous frameshift variant in an alternatively spliced..:

Yüksel, Zafer ; Vogel, Florian ; Alhashem, Amal M....
Clinical Genetics.  95 (2019)  5 - p. 631-633 , 2019
Link: https://doi.org/10.1111/..
 
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15

Expanding the allelic spectrum of ELOVL4‐related autosomal ..:

Alabdulrazzaq, Fatima ; Alanzi, Talal ; Al‐Balool, Haya H...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10724518/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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