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List of works by Karim Ouldim

Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects

scientific article published on 01 October 2020

Associations between nutritional factors and KRAS mutations in colorectal cancer: a systematic review

scientific article published on 28 July 2020

Chromosome markers: case report

scientific article published on 18 July 2013

Cover Image, Volume 173A, Number 9, September 2017.

scientific article published in September 2017

GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot

scientific article published on 01 December 2018

Lynch syndrome: case report and review of the literature

scientific article published on 14 June 2016

Microdeletion syndromes (Williams syndrome and deletion syndrome 22q11) at CHU Hassan II of Fez: report of 3 observations

scientific article published on 12 January 2012

Molecular and presymptomatic analysis of a Moroccan Lynch syndrome family revealed a novel frameshift MLH1 germline mutation

scientific article published on 01 November 2018

NKX2-5 molecular screening and assessment of variant rate and risk factors of secundum atrial septal defect in a Moroccan population

scientific article

Noonan syndrome in diverse populations.

scientific article

Noonan syndrome-causing genes: Molecular update and an assessment of the mutation rate

scientific article published on 18 August 2016

Novel NKX2-5 germline mutation in a Moroccan child with transitional atrio-ventricular septal defect (tAVSD).

scientific article

Pharmacogenetics: what about Morocco?

scientific article published on 10 April 2013

The Cri du Chat syndrome: report of an observation

scientific article

The First Molecular Screening of MLH1 and MSH2 Genes in Moroccan Colorectal Cancer Patients Shows a Relatively High Mutational Prevalence

scientific article published on 25 July 2018

The detection of a novel insertion mutation in exon 2 of the MEFV gene associated with familial mediterranean fever in a moroccan family

scientific article published on 15 June 2017

The first PTPN1 1 mutations in hotspot exons reported in Moroccan children with Noonan syndrome and comparison of mutation rate to previous studies.

scientific article

Williams–Beuren syndrome in diverse populations

scientific article published in May 2018

[Fanconi anemia at the University Hospital (CHU) Hassan II of Fez: about 6 cases].

scientific article published on 4 December 2017

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