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Cherkaoui Jaouad, Imane
69  Ergebnisse:
Personensuche X
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1

Early diagnosis of congenital muscular pathologies using ne..:

El Kadiri, Youssef ; Ratbi, Ilham ; Ouhenach, Mouna...
Egyptian Journal of Medical Human Genetics.  24 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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2

First application of next-generation sequencing in four fam..:

Sahli, Maryem ; Zrhidri, Abdelali ; El Kadiri, Youssef...
Egyptian Journal of Medical Human Genetics.  24 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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3

Next generation sequencing identifies a pathogenic mutation..:

Sahli, Maryem ; Zrhidri, Abdelali ; Boualaoui, Imad...
Journal of Medical Case Reports.  17 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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4

Novel mutation in the TGFBI gene in a Moroccan family with ..:

Benbouchta, Yahya ; Cherkaoui Jaouad, Imane ; Tazi, Habiba...
BMC Medical Genomics.  14 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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5

A novel non sense mutation in WDR62 causes autosomal recess..:

Cherkaoui Jaouad, Imane ; Zrhidri, Abdelali ; Jdioui, Wafaa...
BMC Medical Genetics.  19 (2018)  1 - p. , 2018
Link: https://doi.org/10.1186/..
 
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6

Novel splice site mutation in CNNM4 gene in a family with J..:

Cherkaoui Jaouad, Imane ; Lyahyai, Jaber ; Guaoua, Soukaina...
European Journal of Medical Genetics.  60 (2017)  5 - p. 239-244 , 2017
Link: https://doi.org/10.1016/..
 
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7

Non lethal Raine syndrome and differential diagnosis:

Elalaoui, Siham Chafai ; Al-Sheqaih, Nada ; Ratbi, Ilham...
European Journal of Medical Genetics.  59 (2016)  11 - p. 577-583 , 2016
Link: https://doi.org/10.1016/..
 
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8

Further evidence for causal FAM20A mutations and first case..:

Cherkaoui Jaouad, Imane ; El Alloussi, Mustapha ; Chafai El alaoui, Siham...
BMC Oral Health.  15 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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9

Hyaline fibromatosis syndrome with mutation c.1074delT of t..:

Cherkaoui Jaouad, Imane ; Guaoua, Soukaina ; Hajjioui, Aicha.
Journal of Medical Case Reports.  8 (2014)  1 - p. , 2014
Link: https://doi.org/10.1186/..
 
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10

Omenn syndrome:

Cherkaoui Jaouad, Imane ; Ouldim, K. ; Ali Ou Alla, S....
The Indian Journal of Pediatrics.  , 2008
Link: https://doi.org/10.1007/..
 
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11

MEFV mutations in Moroccan patients suffering from familial..:

Belmahi, Latifa ; Cherkaoui, Imane Jaouad ; Hama, Iman.
Rheumatology International.  32 (2011)  4 - p. 981-984 , 2011
Link: https://doi.org/10.1007/..
 
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12

Mutational spectrum of BRCA1/2 genes in Moroccan patients w..:

Elalaoui, Siham Chafai ; Laarabi, Fatima Zohra ; Afif, Lamiae...
Breast Cancer Research and Treatment.  194 (2022)  1 - p. 187-198 , 2022
Link: https://doi.org/10.1007/..
 
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13

Application of next generation sequencing in genetic counse..:

Ouhenach, Mouna ; Zrhidri, Abdelali ; Jaouad, Imane Cherkaoui..
BMC Medical Genetics.  21 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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14

Molecular diagnosis of dystrophinopathies in Morocco and re..:

EL Kadiri, Youssef ; Selouani, Yassir ; Ratbi, Ilham...
Clinica Chimica Acta.  506 (2020)  - p. 28-32 , 2020
Link: https://doi.org/10.1016/..
 
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15

Surprisingly good outcome in antenatal diagnosis of severe ..:

Wallis, Mathew ; Baumer, Alessandra ; Smaili, Wiam...
European Journal of Medical Genetics.  61 (2018)  4 - p. 189-196 , 2018
Link: https://doi.org/10.1016/..
 
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