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Hussein, Ibtessam Ramzi
15  Ergebnisse:
Personensuche X
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1

Identification of Extremely Rare Pathogenic CNVs by Array C..:

Karim, Sajjad ; Hussein, Ibtessam Ramzi ; Schulten, Hans-Juergen...
Children.  10 (2023)  4 - p. 662 , 2023
Link: https://doi.org/10.3390/..
 
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2

Application of array comparative genomic hybridization (arr..:

Hussein, Ibtessam Ramzi ; Chaudhary, Adeel G. ; Bassiouni, Randa...
BMC Genomics.  15 (2014)  S2 - p. , 2014
Link: https://doi.org/10.1186/..
 
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3

Identification of Extremely Rare Pathogenic CNVs by Array C..:

Karim, Sajjad ; Hussein, Ibtessam Ramzi ; Schulten, Hans-Juergen...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10136417/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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4

Identification of Extremely Rare Pathogenic CNVs by Array C..:

Sajjad Karim ; Ibtessam Ramzi Hussein ; Hans-Juergen Schulten...
https://www.mdpi.com/2227-9067/10/4/662.  , 2023
Link: https://doi.org/10.3390/..
 
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5

Identification of Extremely Rare Pathogenic CNVs by Array C..:

Sajjad Karim ; Ibtessam Ramzi Hussein ; Hans-Juergen Schulten...
Child Neurology.  , 2023
Link: https://doi.org/10.3390/..
 
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6

Identification of De Novo and Rare Inherited Copy Number Va..:

Hussein, Ibtessam R. ; Bader, Rima S. ; Chaudhary, Adeel G....
Pediatric Cardiology.  39 (2018)  5 - p. 924-940 , 2018
Link: https://doi.org/10.1007/..
 
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7

Characterization of familial breast cancer in Saudi Arabia:

Merdad, Adnan ; Gari, Mamdooh A ; Hussein, Shireen...
BMC Genomics.  16 (2015)  S1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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8

Application of molecular genetics techniques for detecting ..:

Magbooli, Afaf ; Huwait, Etimad ; Hussein, Ibtessam R..
BMC Genomics.  15 (2014)  S2 - p. , 2014
Link: https://doi.org/10.1186/..
 
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9

Detection of rare single nucleotide variants affecting gene..:

Hussein, Shireen ; Merdad, Adnan ; Al-Maghrabi, Jaudah...
BMC Genomics.  15 (2014)  S2 - p. , 2014
Link: https://doi.org/10.1186/..
 
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10

Molecular Diagnosis of Fragile X Syndrome Using Methylation..:

Chaudhary, Adeel G. ; Hussein, Ibtessam R. ; Abuzenadah, Adel...
Pediatric Neurology.  50 (2014)  4 - p. 368-376 , 2014
Link: https://doi.org/10.1016/..
 
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11

ThalassoChip, an array mutation and single nucleotide polym..:

Shammas, Christos ; Papasavva, Thessalia ; Felekis, Xenia...
cclm.  48 (2010)  12 - p. 1713-1718 , 2010
Link: https://doi.org/10.1515/..
 
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12

Loss-of-function mutations in the cathepsin C gene result i..:

Toomes, Carmel ; James, Jacqueline ; Wood, A. Joseph...
Nature Genetics.  23 (1999)  4 - p. 421-424 , 1999
Link: https://doi.org/10.1038/..
 
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13

Molecular characterization of β-thalassemia in Egyptians:

Hussein, Ibtessam R. ; Temtamy, Samia A. ; El-Beshlawy, Amal...
Human Mutation.  2 (1993)  1 - p. 48-52 , 1993
Link: https://doi.org/10.1002/..
 
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14

Egyptian Society of Liver Cancer Recommendation Guidelines ..:

Omar, Ashraf ; Kaseb, Ahmed ; Elbaz, Tamer...
Journal of Hepatocellular Carcinoma.  10 (2023)  - p. 2101-2102 , 2023
Link: https://doi.org/10.2147/..
 
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15

Egyptian Society of Liver Cancer Recommendation Guidelines ..:

Omar, Ashraf ; Kaseb, Ahmed ; Elbaz, Tamer...
Journal of Hepatocellular Carcinoma.  10 (2023)  - p. 1547-1571 , 2023
Link: https://doi.org/10.2147/..
 
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