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Showing results (1211-1220 of 1,215) with videos related to

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Nature Communications|September 4, 2019
The molecular origin and taxonomy of mucinous ovarian carcinomaDane Cheasley, Matthew J Wakefield, Georgina L Ryland, et al.
Human Mutation|March 1, 2019
SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported IndividualsBobby G Ng, Paulina Sosicka, Satish Agadi, et al.
Human Molecular Genetics|January 10, 2014
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritanceFrank J Kaiser, Morad Ansari, Diana Braunholz, et al.
The Journal of Clinical Investigation|September 18, 2025
PTBP1 variants displaying altered nucleocytoplasmic distribution are responsible for a neurodevelopmental disorder with skeletal dysplasiaAymeric Masson, Julien Paccaud, Martina Orefice, et al.
ACS Nano|September 4, 2025
33 Unresolved Questions in Nanoscience and NanotechnologyChad A Mirkin, Sarah Hurst Petrosko, Natalie Artzi, et al.
Pageof 122

Showing results (1211-1220 of 1,215) with videos related to

Sort By:
Pageof 122
You have reached the last page of results.This site can display upto 1,215 results.
Nature Communications|September 4, 2019
The molecular origin and taxonomy of mucinous ovarian carcinomaDane Cheasley, Matthew J Wakefield, Georgina L Ryland, et al.
Human Mutation|March 1, 2019
SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported IndividualsBobby G Ng, Paulina Sosicka, Satish Agadi, et al.
Human Molecular Genetics|January 10, 2014
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritanceFrank J Kaiser, Morad Ansari, Diana Braunholz, et al.
The Journal of Clinical Investigation|September 18, 2025
PTBP1 variants displaying altered nucleocytoplasmic distribution are responsible for a neurodevelopmental disorder with skeletal dysplasiaAymeric Masson, Julien Paccaud, Martina Orefice, et al.
ACS Nano|September 4, 2025
33 Unresolved Questions in Nanoscience and NanotechnologyChad A Mirkin, Sarah Hurst Petrosko, Natalie Artzi, et al.
Pageof 122