Complex translocation leading to13q interstitial deletion in a Moroccan child with retinoblastoma and intellectual disability-Reference-Cited by-同舟云学术

Complex translocation leading to13q interstitial deletion in a Moroccan child with retinoblastoma and intellectual disability

Published:2022-06-06 Issue:5 Volume:43 Page:689-692
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

EL Amrani Zhour¹²,Elalaoui Siham Chafai¹²,Jdioui Wafae³,Sbiti Aziza¹²,Ratbi Ilham¹²,Liehr Thomas⁴,Sefiani Abdelaziz¹²,Natiq Abdelhafid¹²

Affiliation:

1. RABAT Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco

2. Département de Génétique Médicale, Institut National d’Hygiène, Rabat, Morocco

3. médicale, Centre des consultations et des explorations externes, Hopital d’enfants, CHU Ibn SinaConsultation de génétique, Rabat, Marocco

4. Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Jena, Germany

Funder

reported

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2022.2083183

Reference20 articles.

1. Retinoblastoma in Great Britain 1969-80: incidence, treatment, and survival.

2. 13q deletion syndrome resulting from balanced chromosomal rearrangement in father: the significance of parental karyotyping

3. Rétinoblastome : résultats préliminaires du protocole national de prise en charge au CHU de Casablanca

4. Recurrent Sporadic Bilateral Retinoblastoma in a Child with 13q Deletion Syndrome

5. FISH banding methods: applications in research and diagnostics