Publications by authors named "Sarah Guterman"

Claim this Profile
C
COG6-related prenatal phenotype (CDG2L): Clinico-pathological report and review of the literature.
Sarah Guterman, Agnese Feresin, Lucile Boutaud, Clémence Jacquin, Stanislas Lyonnet

Mol Genet Genomic Med· April 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
1
1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients.
Clémence Jacquin, Emilie Landais, Céline Poirsier, Alexandra Afenjar, Ahmad Akhavi, Sarah Guterman

Am J Med Genet A· February 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Bi-allelic pathogenic variations in DNAJB11 cause Ivemark II syndrome, a renal-hepatic-pancreatic dysplasia.
Penelope Jordan, Christelle Arrondel, Bettina Bessières, Aude Tessier, Tania Attié-Bitach, Sarah Guterman

Kidney Int· February 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Prenatal findings in 1p36 deletion syndrome: New cases and a literature review.
Sarah Guterman, Claire Beneteau, Sylvia Redon, Céline Dupont, Chantal Missirian

Prenat Diagn· September 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Chromosomal microarray analysis in fetuses with an isolated congenital heart defect: A retrospective, nationwide, multicenter study in France.
Marguerite Hureaux, Sarah Guterman, Bérénice Hervé, Marianne Till, Sylvie Jaillard

Prenat Diagn· May 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Autoimmune disorders but not heparin are associated with cell-free fetal DNA test failure.
Yohann Dabi, Sarah Guterman, Jacques C Jani, Alexandra Letourneau, Adèle Demain

J Transl Med· December 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
First prenatal diagnosis of a 'pure' 9q34.3 deletion (Kleefstra syndrome): A case report and literature review.
Sarah Guterman, Bérénice Hervé, Julie Rivière, Delphine Fauvert, Patrice Clement

J Obstet Gynaecol Res· March 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Intervention to decrease glyburide use in elderly patients with renal insufficiency.
Sherrie L Aspinall, Xinhua Zhao, Chester B Good, Roslyn A Stone, Joy Boresi, Sarah Guterman

Am J Geriatr Pharmacother· February 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis