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Author/Creator Guterman, Sarah

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

Authors:
Jacquin, Clémence; Landais, Emilie; Poirsier, Céline; Afenjar, Alexandra; Akhavi, Ahmad; Bednarek, Nathalie; Bénech, Caroline; Bonnard, Adeline; Bosquet, Damien; Burglen, Lydie; Callier, Patrick; Chantot‐Bastaraud, Sandra; Coubes, Christine; Coutton, Charles; Delobel, Bruno; Descharmes, Margaux; ...
Journal:
American journal of medical genetics
Issue:
Volume 191:Issue 2(2023)
Page Start:
445
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

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

Authors:
Hureaux, Marguerite; Guterman, Sarah; Hervé, Bérénice; Till, Marianne; Jaillard, Sylvie; Redon, Sylvie; Valduga, Myléne; Coutton, Charles; Missirian, Chantal; Prieur, Fabienne; Simon‐Bouy, Brigitte; Beneteau, Claire; Kuentz, Paul; Rooryck, Caroline; Gruchy, Nicolas; Marle, Nathalie; Plutino, Morg...
Journal:
Prenatal diagnosis
Issue:
Volume 39:Number 6(2019)
Page Start:
464
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Prenatal findings in 1p36 deletion syndrome: New cases and a literature review. (5th July 2019)

Authors:
Guterman, Sarah; Beneteau, Claire; Redon, Sylvia; Dupont, Céline; Missirian, Chantal; Jaeger, Pauline; Herve, Berenice; Jacquin, Clémence; Douet‐Guilbert, Nathalie; Till, Marianne; Tabet, Anne‐Claude; Moradkhani, Kamran; Malan, Valérie; Doco‐Fenzy, Martine; Vialard, François
Journal:
Prenatal diagnosis
Issue:
Volume 39:Number 10(2019)
Page Start:
871
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗