Showing results (331-340 of 339) with videos related to
Sort By:
Pageof 34
You have reached the last page of results.This site can display upto 339 results.
Human Mutation|October 11, 2018
Global genetic insight contributed by consanguineous Pakistani families segregating hearing lossElodie M Richard, Regie Lyn P Santos-Cortez, Rabia Faridi, et al.American Journal of Human Genetics|January 9, 2008
Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35Rob W J Collin, Ersan Kalay, Muhammad Tariq, et al.European Journal of Human Genetics : EJHG|December 11, 2014
Challenges and solutions for gene identification in the presence of familial locus heterogeneityAtteeq U Rehman, Regie Lyn P Santos-Cortez, Meghan C Drummond, et al.Nature Genetics|October 2, 2012
Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48Saima Riazuddin, Inna A Belyantseva, Arnaud P J Giese, et al.American Journal of Human Genetics|April 2, 2013
Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered proteaseEmma M Jenkinson, Atteeq U Rehman, Tom Walsh, et al.Clinical Genetics|May 22, 2024
Clinical and genetic investigation of 14 families with various forms of short stature syndromesFati Ullah Khan, Hammal Khan, Kifayat Ullah, et al.American Journal of Human Genetics|January 25, 2011
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42Guntram Borck, Atteeq Ur Rehman, Kwanghyuk Lee, et al.Nature|July 26, 2019
Soil nematode abundance and functional group composition at a global scaleJohan van den Hoogen, Stefan Geisen, Devin Routh, et al.Scientific Data|March 29, 2020
A global database of soil nematode abundance and functional group compositionJohan van den Hoogen, Stefan Geisen, Diana H Wall, et al.Pageof 34