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Annals of Human Genetics|March 10, 2023
The genetic era of childhood cancer: Identification of high-risk patients and germline sequencing approachesOscar Alonso-Luna, Gabriela E Mercado-Celis, Jorge Melendez-Zajgla, et al.Annals of Human Genetics|March 10, 2023
A de novo low-frequency mosaic variant of KIF1A causes hereditary spastic paraplegia: A literature reviewMengyuan Liu, Bing Li, Xiaona Wang, et al.Annals of Human Genetics|April 17, 1998
Genetic analysis of a Japanese patient with butyrylcholinesterase deficiencyK Hidaka, I Iuchi, M Tomita, et al.Annals of Human Genetics|April 17, 1998
A tale of two islands: population history and mitochondrial DNA sequence variation of Bioko and São Tomé, Gulf of GuineaE Mateu, D Comas, F Calafell, et al.Annals of Human Genetics|April 17, 1998
Localization of the fast skeletal muscle troponin I gene (TNNI2) to 11p15.5: genes for troponin I and T are organized in pairsP J Barton, P J Townsend, N J Brand, et al.Annals of Human Genetics|April 17, 1998
DNA polymorphisms of apolipoprotein B in the population of SenegalM Chauffert, J Larghero, K Ngohou-Botum, et al.Annals of Human Genetics|July 1, 1976
Visual classification of banded human chromosomes. I. Karyotyping compared with classification of isolated chromosomesC Lundsteen, A M Lind, E GranumAnnals of Human Genetics|July 1, 1976
C- and Q-band polymorphisms in the chromosomes of three human populationsK E Buckton, M L O'Riordan, P A Jacobs, et al.Annals of Human Genetics|August 28, 2025
Prevalence of the Main Human Genetic Variants Related to Resistance to Malaria in a Population of the Colombian Pacific CoastDiana Carolina Ortega, María Paula Arango, Sergio Cañón, et al.Annals of Human Genetics|October 1, 1984
Mutation and selection in the marker (X) syndrome. A hypothesisF VogelPageof 231