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European Journal of Human Genetics : EJHG|September 28, 2019
Functional variants in ADH1B and ALDH2 are non-additively associated with all-cause mortality in Japanese populationSaori Sakaue, Masato Akiyama, Makoto Hirata, et al.
European Journal of Human Genetics : EJHG|February 18, 2011
Parents' and children's communication about genetic risk: a qualitative study, learning from families' experiencesAlison Metcalfe, Gill Plumridge, Jane Coad, et al.
European Journal of Human Genetics : EJHG|June 12, 2014
Impact on parents of HLA-DQ2/DQ8 genotyping in healthy children from coeliac familiesMargreet M S Wessels, Sabine L Vriezinga, Sybille Koletzko, et al.
European Journal of Human Genetics : EJHG|August 27, 2015
Children with sex chromosome trisomies: parental disclosure of genetic statusNikki C Gratton, Jessica Myring, Prisca Middlemiss, et al.
European Journal of Human Genetics : EJHG|October 8, 2004
A novel PTPN11 gene mutation bridges Noonan syndrome, multiple lentigines/LEOPARD syndrome and Noonan-like/multiple giant cell lesion syndromeAnna Sarkozy, Maria Gabriela Obregon, Emanuela Conti, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
Inheritance of human longevity in IcelandH Gudmundsson, D F Gudbjartsson, M Frigge, et al.
European Journal of Human Genetics : EJHG|July 17, 2023
Nemaline myopathy: reclassification of previously reported variants according to ACMG guidelines, and report of novel genetic variantsAlireza Haghighi, Zahra Alvandi, Yalda Nilipour, et al.
European Journal of Human Genetics : EJHG|June 26, 2023
Episignature analysis of moderate effects and mosaicsKonrad Oexle, Michael Zech, Lara G Stühn, et al.
European Journal of Human Genetics : EJHG|August 1, 2023
Consanguinity and willingness to perform premarital genetic screening in SudanYasir Ahmed Mohammed Elhadi, Salma S Alrawa, Esraa S A Alfadul, et al.
European Journal of Human Genetics : EJHG|July 28, 2023
Clinical trio genome sequencing facilitates the interpretation of variants in cancer predisposition genes in paediatric tumour patientsChristopher Schroeder, Ulrike Faust, Luisa Krauße, et al.
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