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You searched for: Author/Creator Till, M.

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1. A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes. (12th February 2014)

3. Assessment of Transformed Properties In Vitro and of Tumorigenicity In Vivo in Primary Keratinocytes Cultured for Epidermal Sheet Transplantation. (1st September 2010)

8. Genetic counselling difficulties and ethical implications of incidental findings from array‐CGH: a 7‐year national survey. Issue 5 (4th January 2016)

9. Incidental findings on array comparative genomic hybridization: detection of carrier females of dystrophinopathy without any family history. (21st July 2014)

10. Mapping of chromosomal balanced rearrangements by whole-genome sequencing identifies genes involved in epilepsy. (June 2017)