Showing results (121-130 of 352) with videos related to

Sort By:
Pageof 36
British Journal of Cancer|September 8, 2017
Aldehyde dehydrogenase 1B1: a novel immunohistological marker for colorectal cancerAkiko Matsumoto, John Arcaroli, Ying Chen, et al.
American Journal of Medical Genetics|October 1, 1993
Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndromeJ Clayton-Smith, D J Driscoll, M F Waters, et al.
Clinical Genetics|September 8, 2011
Systematic screening of FBN1 gene unclassified missense variants for splice abnormalitiesD O Robinson, F Lin, M Lyon, et al.
Clinical Dysmorphology|July 1, 1994
Radial ray defects, renal ectopia, duodenal atresia and hydrocephalus: the extended spectrum for Fanconi anaemiaD G Evans, H C Rees, A Spreadborough, et al.
JACC. Case Reports|December 14, 2023
Valve-in-Valve Transcatheter Aortic Valve Replacement During Second Trimester of PregnancyAparna Sajja, Maya Dassanayake, Iris Abrahantes Morales, et al.
American Journal of Medical Genetics|September 15, 1992
Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndromeJ Clayton-Smith, T Webb, S A Robb, et al.
Human Mutation|December 19, 2001
A survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individualsN Elanko, J S Sibbring, K A Metcalfe, et al.
Plos One|July 1, 2016
Low-Cost 3D Printers Enable High-Quality and Automated Sample Preparation and Molecular DetectionKamfai Chan, Mauricio Coen, Justin Hardick, et al.
Pediatric Radiology|August 29, 2025
Liver stiffness measured by MR elastography in children and adults with Fontan circulation: defining expected values and clinical associationsJulia Razavi, Andrew T Trout, Cara E Morin, et al.
European Journal of Medical Genetics|February 21, 2012
Another cause of vaccine encephalopathy: a case of Angelman syndromeJan Novy, Claudia B Catarino, Krishna Chinthapalli, et al.
Pageof 36