Showing results (1-10 of 68) with videos related to

Sort By:
Pageof 7
European Journal of Human Genetics : EJHG|December 20, 2017
WISExome: a within-sample comparison approach to detect copy number variations in whole exome sequencing dataRoy Straver, Marjan M Weiss, Quinten Waisfisz, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|April 28, 2009
Chromosomal changes in sporadic and familial head and neck paragangliomasMaría A Sevilla, Mario A Hermsen, Marjan M Weiss, et al.
Cellular Oncology : the Official Journal of the International Society for Cellular Oncology|December 30, 2004
Genomic alterations in primary gastric adenocarcinomas correlate with clinicopathological characteristics and survivalMarjan M Weiss, Ernst J Kuipers, Cindy Postma, et al.
Molecular Vision|August 10, 2012
Identification of a novel FBN1 gene mutation in a large Pakistani family with Marfan syndromeShazia Micheal, Muhammad Imran Khan, Farah Akhtar, et al.
European Journal of Medical Genetics|June 13, 2008
A 400kb duplication, 2.4Mb triplication and 130kb duplication of 9q34.3 in a patient with severe mental retardationAntoinet C J Gijsbers, Emilia K Bijlsma, Marjan M Weiss, et al.
Cellular Oncology : the Official Journal of the International Society for Cellular Oncology|March 9, 2010
Relevance of germline mutation screening in both familial and sporadic head and neck paraganglioma for early diagnosis and clinical managementMario A Hermsen, María A Sevilla, José Luis Llorente, et al.
European Journal of Human Genetics : EJHG|June 15, 2007
Genotype-phenotype correlations in 19 Dutch cases with APC gene deletions and a literature reviewMaartje Nielsen, Elsa Bik, Frederik J Hes, et al.
Human Genetics|May 29, 2015
First genetic analysis of aneurysm genes in familial and sporadic abdominal aortic aneurysmKoen M van de Luijtgaarden, Daphne Heijsman, Alessandra Maugeri, et al.
Molecular Genetics & Genomic Medicine|November 29, 2018
Autosomal dominant Marfan syndrome caused by a previously reported recessive FBN1 variantEline Overwater, Rifka Efrat, Daniela Q C M Barge-Schaapveld, et al.
Journal of Pediatric Hematology/Oncology|May 7, 2002
Genetic alterations in childhood medulloblastoma analyzed by comparative genomic hybridizationErna M C Michiels, Marjan M Weiss, Jan M N Hoovers, et al.
Pageof 7