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Informations du chercheur

Nom complet

ABOUSSAIR NISRINE

Grade

PES

Spécialité

Génétique

Thématique de recherche

Maladies génétiques/RARES

Laboratoire

Laboratoire DE RECHERCHE L'ENFANCE, LA SANTE ET LE DEVELOPPEMENT DURABLE

Établissement

Non spécifié

Ouvrages (0 au total)

Aucun ouvrage disponible.

Projets (0 au total)

Aucun projet disponible.

Communications (118 au total)

Clinical and genetic aspects of Leber congenital amaurosis: First Moroccan series

Manifestation: The first international congress of the Moroccan Society of Genomics and Human Genetics (SM2GH) and the third of School of Immunogenetic December , 19th 2019

Date: 2019-12-19

Organisation: Agadir

Trisomy 18 : First Series of the Genetics Department of Marrakech

Manifestation: the first International Congress of the Moroccan Society of Genomics and Human Genetics (SM2GH) & Third School of Immunogenetics (SIG)

Date: 2019-12-19

Organisation: Agadir

Cytogenetic aspects of chronic myeloid leukemia: a series of 147 cases

Manifestation: The first international congress of the Moroccan Society of Genomics and Human Genetics (SM2GH) and the third of School of Immunogenetic December , 19th 2019

Date: 2019-12-19

Organisation: Agadir

1- Man with uterus: about three cases

Manifestation: First International Congress of the Moroccan Society of Genomic and Human Genetics and the third edition of the School of immunogenetics 19-21 December 2019

Date: 2019-12-19

Organisation: Agadir

Bilan génétique des surdités de l'enfant

Manifestation: Atelier ORL organisé par l'association de pédiatrie de la région Tensift Alhaouz

Date: 2019-12-14

Organisation: Marrakech

Oncogénétique et cancer de la prostate

Manifestation: Rencontre d'onco Urologie de Marrakech (ROUM)

Date: 2019-11-02

Organisation: Marrakech

The molecular diagnosis of duchene and becker myopathy by multipex-PCR : first series of the genetics department of Mohammed VI University Hospital of Marrakech.

Manifestation: 2nd International Scientific Conference for Research and Ethics

Date: 2019-04-19

Organisation: Taroudant

Syndrome de prader wili :première série du service de génétique du chu Mohammed VI de Marrakech

Manifestation: 2nd International Scientific Conference for Research and Ethics

Date: 2019-04-19

Organisation: Taroudant

Mutation faux sens du gène MECP2 chez 02 patients atteints du syndrome de RETT

Manifestation: 2nd International Scientific Conference for Research and Ethics

Date: 2019-04-19

Organisation: Taroudant