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Muriel Payet

10

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77

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Saint-Joseph – Rivière des Remparts, Caverne Lépinay. Sondage (2015)

2020
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6q16.3q23.3 duplication associated with Prader-Willi-like syndrome.

2015 Molecular Cytogenetics
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An Improved Method to Extract DNA from 1 ml of Uncultured Amniotic Fluid from Patients at Less than 16 Weeks’ Gestation

2013 PLOS ONE
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A prenatal case of inverted duplication with terminal deletion of 5p not including the cat‐like cry critical region

2011 American Journal of Medical Genetics Part A
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Refining the critical region for congenital diaphragmatic hernia on chromosome 15q26 from the study of four fetuses.

2011 Prenatal Diagnosis
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17q21.31 microdeletion in a patient with pituitary stalk interruption syndrome.

2011 European Journal of Medical Genetics
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Search for genomic imbalances in a cohort of 20 patients with oral–facial–digital syndromes negative for mutations and large rearrangements in the OFD1 gene

2009 American Journal of Medical Genetics Part A
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