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Sarah Guterman

4PUBLICATIONS

8CO-AUTHORS

Gene mappingNeonatologyGene expression (incl. microarray and other genome-wide approaches)

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Publications (4)

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|Nov 12, 2022

1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients.

Clémence Jacquin, Emilie Landais, Céline Poirsier

|Jun 08, 2019

Prenatal findings in 1p36 deletion syndrome: New cases and a literature review.

Sarah Guterman, Claire Beneteau, Sylvia Redon

|Mar 22, 2019

Chromosomal microarray analysis in fetuses with an isolated congenital heart defect: A retrospective, nationwide, multicenter study in France.

Marguerite Hureaux, Sarah Guterman, Bérénice Hervé

|Nov 22, 2017

First prenatal diagnosis of a 'pure' 9q34.3 deletion (Kleefstra syndrome): A case report and literature review.

Sarah Guterman, Bérénice Hervé, Julie Rivière

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Frequent Collaborators

2 joint publications

Paul Kuentz

2 joint publications

Valérie Malan

1 joint publications

Kamran Moradkhani

1 joint publications

Clémence Jacquin

1 joint publications

Guillaume Jouret

1 joint publications

Jonathan Levy

1 joint publications

Jacques Puechberty

1 joint publications

Damien Sanlaville

Frequent Collaborators

2 joint publications

Paul Kuentz

2 joint publications

Valérie Malan

1 joint publications

Kamran Moradkhani

1 joint publications

Clémence Jacquin

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