Search Results - "Altaraihi, Mays" :: K.UTB vyhledávací portál

Loading…

A new family with a homozygous nonsense variant in NTHL1 further delineated the clinical phenotype of NTHL1-associated polyposis

by Altaraihi, Mays, Gerdes, Anne-Marie, Wadt, Karin
Published in Human genome variation (10.10.2019)

Get full text

Journal Article

Loading…

Prevalence of Pathogenic Germline DICER1 Variants in Young Individuals Thyroidectomised Due to Goitre - A National Danish Cohort

by Altaraihi, Mays, Hansen, Thomas van Overeem, Santoni-Rugiu, Eric, Rossing, Maria, Rasmussen, Åse Krogh, Gerdes, Anne-Marie, Wadt, Karin
Published in Frontiers in endocrinology (Lausanne) (06.09.2021)

Get full text

Journal Article

Loading…

A family with a congenital DICER1 mutation

by Altaraihi, Mays, Pedersen, Jens, Rossing, Maria, Gedes, Anne-Marie, Wadt, Karin
Published in Ugeskrift for læger (18.06.2018)

Get more information

Journal Article

A new family with a homozygous nonsense variant in NTHL1 further delineated the clinical phenotype of NTHL1-associated polyposis

Prevalence of Pathogenic Germline DICER1 Variants in Young Individuals Thyroidectomised Due to Goitre - A National Danish Cohort

A family with a congenital DICER1 mutation

Refine Results

Format

Subject Area

Topic

Language

Year of Publication

Database