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American Journal of Human Genetics|April 1, 1986
The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1M E Goode, P vanTuinen, D H Ledbetter, et al.American Journal of Human Genetics|September 4, 2018
Fetal-Not Maternal-APOL1 Genotype Associated with Risk for Preeclampsia in Those with African AncestryKimberly J Reidy, Rebecca C Hjorten, Claire L Simpson, et al.American Journal of Human Genetics|May 29, 2018
Heterozygous Truncating Variants in POMP Escape Nonsense-Mediated Decay and Cause a Unique Immune Dysregulatory SyndromeM Cecilia Poli, Frédéric Ebstein, Sarah K Nicholas, et al.American Journal of Human Genetics|August 1, 1986
Determining the mode of inheritance of RFLP-associated diseases using the affected sib-pair methodG ThomsonAmerican Journal of Human Genetics|January 1, 1986
The analysis of multiple polymorphic loci on a single human chromosome to exclude linkage to inherited disease: cystic fibrosis and chromosome 4M Farrall, P Scambler, P North, et al.American Journal of Human Genetics|May 5, 2018
The Post-GWAS Era: From Association to FunctionMichael D Gallagher, Alice S Chen-PlotkinAmerican Journal of Human Genetics|May 5, 2018
Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein ArmsInga M Höben, Rim Hjeij, Heike Olbrich, et al.American Journal of Human Genetics|March 11, 2000
Functional analysis of the neurofibromatosis type 2 protein by means of disease-causing point mutationsR P Stokowski, D R CoxAmerican Journal of Human Genetics|March 11, 2000
A locus for brachydactyly type A-1 maps to chromosome 2q35-q36X Yang, C She, J Guo, et al.American Journal of Human Genetics|March 11, 2000
Multipoint estimation of genetic maps for human trisomies with one parent or other partial dataE Feingold, A S Brown, S L ShermanPageof 979