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Ben Aissa-Haj, Jihenne
15  results:
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1

A regionally based precision medicine implementation initia..:

Hamdi, Yosr ; Boujemaa, Maroua ; Ben Aissa-Haj, Jihenne...
Translational Oncology.  44 (2024)  - p. 101940 , 2024
Link: https://doi.org/10.1016/..
 
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2

CDH1 Germline Variants in a Tunisian Cohort with Hereditary..:

Ben Aissa-Haj, Jihenne ; Kabbage, Maria ; Othmen, Houcemeddine...
Genes.  13 (2022)  3 - p. 400 , 2022
Link: https://doi.org/10.3390/..
 
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3

The Identification of Large Rearrangements Involving Intron..:

Ben Aissa-Haj, Jihenne ; Pinheiro, Hugo ; Cornelis, François...
Genes.  13 (2022)  12 - p. 2213 , 2022
Link: https://doi.org/10.3390/..
 
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4

A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrom..:

Kabbage, Maria ; Ben Aissa-Haj, Jihenne ; Othman, Houcemeddine...
Genes.  13 (2022)  8 - p. 1355 , 2022
Link: https://doi.org/10.3390/..
 
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5

The Identification of Large Rearrangements Involving Intron..:

Ben Aissa-Haj, Jihenne ; Pinheiro, Hugo ; Cornelis, François...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9778491/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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6

A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrom..:

Kabbage, Maria ; Ben Aissa-Haj, Jihenne ; Othman, Houcemeddine...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407052/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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7

A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrom..:

Kabbage, Maria ; Ben Aissa-Haj, Jihenne ; Othman, Houcemeddine...
info:eu-repo/semantics/altIdentifier/doi/10.3390/genes13081355.  , 2022
Link: https://amu.hal.science/..
 
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8

A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrom..:

Kabbage, Maria ; Ben Aissa-Haj, Jihenne ; Othman, Houcemeddine...
info:eu-repo/semantics/altIdentifier/doi/10.3390/genes13081355.  , 2022
Link: https://hal-amu.archives..
 
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9

CDH1 Germline Variants in a Tunisian Cohort with Hereditary..:

Jihenne Ben Aissa-Haj ; Maria Kabbage ; Houcemeddine Othmen...
https://www.mdpi.com/2073-4425/13/3/400.  , 2022
Link: https://doi.org/10.3390/..
 
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10

CDH1 Germline Variants in a Tunisian Cohort with Hereditary..:

Jihenne Ben Aissa-Haj ; Maria Kabbage ; Houcemeddine Othmen...
Molecular Genetics and Genomics.  , 2022
Link: https://doi.org/10.3390/..
 
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11

The Identification of Large Rearrangements Involving Intron..:

Jihenne Ben Aissa-Haj ; Hugo Pinheiro ; François Cornelis...
Molecular Genetics and Genomics.  , 2022
Link: https://doi.org/10.3390/..
 
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12

CDH1 and CTNNA1 Genetic Screening in Tunisian Patients with..:

Aissa-Haj, Jihenne, Ben ; Kabbage, Maria ; Othmen, Houcemeddine...
info:eu-repo/semantics/altIdentifier/doi/10.21203/rs.3.rs-617841/v1.  , 2022
Link: https://riip.hal.science..
 
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13

The Identification of Large Rearrangements Involving Intron..:

Jihenne Ben Aissa-Haj ; Hugo Pinheiro ; François Cornelis...
https://www.mdpi.com/2073-4425/13/12/2213.  , 2022
Link: https://doi.org/10.3390/..
 
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14

A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrom..:

Maria Kabbage ; Jihenne Ben Aissa-Haj ; Houcemeddine Othman...
https://www.mdpi.com/2073-4425/13/8/1355.  , 2022
Link: https://doi.org/10.3390/..
 
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15

A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrom..:

Maria Kabbage ; Jihenne Ben Aissa-Haj ; Houcemeddine Othman...
Molecular Genetics and Genomics.  , 2022
Link: https://doi.org/10.3390/..
 
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