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You searched for: Author/Creator Vialard, François

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1. 1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients. Issue 2 (11th November 2022)

5. Application of a new molecular technique for the genetic evaluation of products of conception. (20th November 2012)

8. Chromosomal microarray analysis in fetuses with an isolated congenital heart defect: A retrospective, nationwide, multicenter study in France. (29th April 2019)

9. Critical steps for initiating an animal uterine transplantation model in sheep: Experience from a case series. (December 2018)

10. Cryptic splice site poisoning and meiotic arrest caused by a homozygous frameshift mutation in RBMXL2: A case report. (14th September 2022)