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Annals of Human Genetics|October 1, 1986
Very close linkage between D2S1 and ACP1 on chromosome 2pR A Lothe, T Gedde-Dahl, B Olaisen, et al.
Annals of Human Genetics|November 15, 2021
Expanding the clinico-molecular spectrum of Angelman syndrome phenotype with the GABRG3 gene: Evidence from methylation and sequencing studiesGayatri R Iyer, Prashant Utage, Radha Rama Devi, et al.
Annals of Human Genetics|August 10, 2019
Using microarray analysis to identify genes and pathways that regulate fetal hemoglobin levelsSiyuan Jia, Wenguang Jia, Shanjuan Yu, et al.
Annals of Human Genetics|October 5, 2019
Xq26 duplications lead to undergrowth or overgrowth via competing pathways including GPC3/GPC4Gaurav K Karna, Kenneth A Myers
Annals of Human Genetics|December 8, 2021
Further evidence of muscle involvement in neurodevelopmental disorder with epilepsy, spasticity, and brain atrophyPurvi Majethia, Michelle C Do Rosario, Parneet Kaur, et al.
Annals of Human Genetics|September 3, 2025
A Novel Variant of STAG1 Gene and Literature ReviewMeihua Xie, Liyun Xie, Jianlong Zhuang, et al.
Annals of Human Genetics|June 11, 2015
Classical and atypical Fibrodysplasia Ossificans Progressiva in IndiaVrisha Madhuri, Mona Santhanam, Legasri K Sugumar, et al.
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