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Al Balwi, Mohammad A.
30  Ergebnisse:
Personensuche X
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1

Identification of CSF3R Mutations in B-Lineage Acute Lympho..:

Rashid, Mamoon ; Alasiri, Abdulrahman ; Al Balwi, Mohammad A....
Genes.  12 (2021)  9 - p. 1326 , 2021
Link: https://doi.org/10.3390/..
 
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2

Identification of CSF3R Mutations in B-Lineage Acute Lympho..:

Rashid, Mamoon ; Alasiri, Abdulrahman ; Al Balwi, Mohammad A...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8470887/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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3

Identification of CSF3R Mutations in B-Lineage Acute Lympho..:

Mamoon Rashid ; Abdulrahman Alasiri ; Mohammad A. Al Balwi...
https://www.mdpi.com/2073-4425/12/9/1326.  , 2021
Link: https://doi.org/10.3390/..
 
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4

Identification of CSF3R Mutations in B-Lineage Acute Lympho..:

Mamoon Rashid ; Abdulrahman Alasiri ; Mohammad A. Al Balwi...
Molecular Genetics and Genomics.  , 2021
Link: https://doi.org/10.3390/..
 
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5

Reliability of Agreement between Insulin, Clonidine, and Gl..:

Al Balwi, Rana ; Al-Qahtani, Mohammad ; Alrowished, Amani K....
Children.  10 (2023)  8 - p. 1381 , 2023
Link: https://doi.org/10.3390/..
 
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6

Identification of Novel Mutations in Colorectal Cancer Pati..:

Almuzzaini, Bader ; Alghamdi, Jahad ; Alomani, Alhanouf...
Journal of Personalized Medicine.  11 (2021)  6 - p. 535 , 2021
Link: https://doi.org/10.3390/..
 
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7

Proteomic and Molecular Assessment of the Common Saudi Vari..:

Alfares, Ahmad ; Alfadhel, Majid ; Mujamammi, Ahmed...
Frontiers in Cell and Developmental Biology.  7 (2020)  - p. , 2020
Link: https://doi.org/10.3389/..
 
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8

Thirteen year retrospective review of the spectrum of inbor..:

Alfadhel, Majid ; Benmeakel, Mohammed ; Hossain, Mohammad Arif...
Orphanet Journal of Rare Diseases.  11 (2016)  1 - p. , 2016
Link: https://doi.org/10.1186/..
 
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9

Two novel homozygous missense mutations in the GDF5 gene ca..:

Al‐Qattan, Mohammad M. ; Al‐Motairi, Muhammed I. ; Al Balwi, Mohammed A.
American Journal of Medical Genetics Part A.  167 (2015)  7 - p. 1621-1626 , 2015
Link: https://doi.org/10.1002/..
 
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10

The unclassified variant: c.2044AD>G, p.T682A (het.) in exo..:

Al-Qattan, Mohammad M. ; Al Balwi, Mohammed A.
Gene.  526 (2013)  2 - p. 471-473 , 2013
Link: https://doi.org/10.1016/..
 
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11

A Report of Two cases of Al-Awadi Raas-Rothschild Syndrome ..:

AlQattan, Mohammad M. ; AlAbdulkareem, Ibrahim ; Ballow, Mariam.
Gene.  527 (2013)  1 - p. 371-375 , 2013
Link: https://doi.org/10.1016/..
 
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12

Liebenberg syndrome is caused by a deletion upstream to the..:

Al-Qattan, Mohammad M. ; Al-Thunayan, Abdullah ; AlAbdulkareem, Ibrahim.
Gene.  524 (2013)  1 - p. 65-71 , 2013
Link: https://doi.org/10.1016/..
 
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13

Transaldolase deficiency: report of 12 new cases and furthe..:

Eyaid, Wafaa ; Al Harbi, Talal ; Anazi, Shamsa...
Journal of Inherited Metabolic Disease.  36 (2013)  6 - p. 997-1004 , 2013
Link: https://doi.org/10.1007/..
 
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14

A novel mutation in the SHH long‐range regulator (ZRS) is a..:

Al‐Qattan, Mohammad M. ; Al Abdulkareem, Ibrahim ; Al Haidan, Yazied.
American Journal of Medical Genetics Part A.  158A (2012)  10 - p. 2610-2615 , 2012
Link: https://doi.org/10.1002/..
 
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15

A novel homozygous missense mutation (c.610G>A, p.Gly204Ser..:

Eyaid, Wafaa ; Al‐Qattan, Mohammad M. ; Al Abdulkareem, Ibrahim..
American Journal of Medical Genetics Part A.  155 (2011)  3 - p. 599-604 , 2011
Link: https://doi.org/10.1002/..
 
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