Results 161 to 170 of about 96,085 (345)
The Mendelian Ratio and Blended Inheritance
The American Naturalist, 1911 THE itdefatio1able efforts of neo-Meidelists lha-ve succeeded in brino11io nu immeruou-s cases of inheritaince, w-hich had previoUslyA bmeen considered incompatible with MAtenidel's law, into their domain by widening the origiinal limitationls. We still haive man instances such as blended inheritance which caii not apparentlyt be liarmionized with the ...
openaire +3 more sources
New Light on Blending and Mendelian Inheritance [PDF]
The American Naturalist, 1916 n ...
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Long‐Read Sequencing: The Third Generation of Diagnostic Testing for Dystonia
Movement Disorders, EarlyView.Abstract Long‐read sequencing methodologies provide powerful capacity to identify all types of genomic variations in a single test. Long‐read platforms such as Oxford Nanopore and PacBio have the potential to revolutionize molecular diagnostics by reaching unparalleled accuracies in genetic discovery and long‐range phasing.
Thomas Wirth +2 more
wiley +1 more source
Insect Molecular Biology, Volume 32, Issue 1, Page 56-68, February 2023., 2023 The introgression of a synthetic sex ratio distortion transgene into two different genetic backgrounds of Anopheles coluzzii by six backcrosses. We showed that the phenotype of the sex ratio distorter is stabile in the introgressed An. coluzzii strains.
Paola Pollegioni +13 more
wiley +1 more source
Non-Mendelian inheritance of macronuclear mutations is gene specific in Paramecium tetraurelia. [PDF]
, 1994 J Scott +3 more
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Movement Disorders, EarlyView.Abstract Background Defects of mitochondrial ATP synthase (ATPase) represent an emerging, yet incompletely understood group of neurodevelopmental diseases with abnormal movements. Objective The aim of this study was to redefine the phenotypic and mutational spectrum of movement disorders linked to the ATPase subunit‐encoding genes ATP5F1A and ATP5F1B ...
Philip Harrer +21 more
wiley +1 more source
Non-Mendelian inheritance patterns and extreme deviation rates of CGG repeats in autism. [PDF]
Genome Res, 2022 Annear DJ +4 more
europepmc +1 more source
Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders [PDF]
, 2002 Ada Hamosh
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Micromanipulation in Paramecium: From non-mendelian inheritance to the outlook for versatile micromachines. [PDF]
J Eukaryot Microbiol, 2022 Haga N.
europepmc +1 more source