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American Journal of Human Genetics|January 1, 1985
Fra(10)(q25): the BrdU effect is substitution-dependentS M Gollin, G P Holmquist, D H LedbetterAmerican Journal of Human Genetics|March 1, 1985
Incidence in Italy, genetic heterogeneity, and segregation analysis of cystic fibrosisG Romeo, M Bianco, M Devoto, et al.American Journal of Human Genetics|March 5, 2021
How science will help us move forward in 2021American Journal of Human Genetics|March 5, 2021
ASHG 2020 Curt Stern Award introduction: Fowzan Sami AlkurayaCynthia C MortonAmerican Journal of Human Genetics|August 1, 1987
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21C R Greenberg, J L Hamerton, M Nigli, et al.American Journal of Human Genetics|August 1, 1987
Multipoint gene mapping using seriation. II. Analysis of simulated and empirical dataK H Buetow, A ChakravartiAmerican Journal of Human Genetics|July 30, 2019
Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental DisordersBjörn Fischer-Zirnsak, Lara Segebrecht, Max Schubach, et al.American Journal of Human Genetics|July 23, 2019
De Novo Missense Variants in WDR37 Cause a Severe Multisystemic SyndromeLinda M Reis, Elena A Sorokina, Samuel Thompson, et al.American Journal of Human Genetics|July 16, 2019
Comparing Within- and Between-Family Polygenic Score PredictionSaskia Selzam, Stuart J Ritchie, Jean-Baptiste Pingault, et al.American Journal of Human Genetics|July 16, 2019
Mutations in ANAPC1, Encoding a Scaffold Subunit of the Anaphase-Promoting Complex, Cause Rothmund-Thomson Syndrome Type 1Norbert F Ajeawung, Thi Tuyet Mai Nguyen, Linchao Lu, et al.Pageof 979