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Human Reproduction (Oxford, England)|September 25, 2023
Good practice recommendations on add-ons in reproductive medicine†, K Lundin, J G Bentzen, et al.
Thrombosis and Haemostasis|October 6, 1998
The molecular basis of antithrombin deficiency in Belgian and Dutch familiesK Jochmans, W Lissens, S Seneca, et al.
Stem Cell Reports|June 11, 2019
Gain of 20q11.21 in Human Pluripotent Stem Cells Impairs TGF-β-Dependent Neuroectodermal CommitmentC Markouli, E Couvreu De Deckersberg, M Regin, et al.
Human Mutation|February 19, 2000
Mutations in the X-linked pyruvate dehydrogenase (E1) alpha subunit gene (PDHA1) in patients with a pyruvate dehydrogenase complex deficiencyW Lissens, L De Meirleir, S Seneca, et al.
Acta Anaesthesiologica Scandinavica|January 21, 2012
Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndromeA V Vanlander, P G Jorens, J Smet, et al.
Biochemical and Biophysical Research Communications|November 9, 2005
Aminoacylase I deficiency: a novel inborn error of metabolismR N Van Coster, E A Gerlo, T G Giardina, et al.
Prenatal Diagnosis|December 18, 2001
Preimplantation genetic diagnosis (PGD), a collaborative activity of clinical genetic departments and IVF centresJ P Geraedts, J Harper, P Braude, et al.
European Journal of Human Genetics : EJHG|December 5, 2017
Recent developments in genetics and medically assisted reproduction: from research to clinical applicationsJ C Harper, K Aittomäki, P Borry, et al.
Human Reproduction Open|September 6, 2019
Recent developments in genetics and medically-assisted reproduction: from research to clinical applications†‡J C Harper, K Aittomäki, P Borry, et al.
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