Laetitia Monteil

Toulouse, 31300, France

Last Updated: 09/26/2026

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Found 11 publications

Exposure to CFTR Modulators During Pregnancy in Cystic Fibrosis: Four Cases to Highlight Neonatal Diagnostic Challenges and Outcomes.

Exposure to CFTR Modulators During Pregnancy in Cystic Fibrosis: Four Cases to Highlight Neonatal Diagnostic Challenges and Outcomes.

Journal: International journal of neonatal screening

Published: July 21, 2025

Noninvasive prenatal diagnosis of genetic diseases induced by triplet repeat expansion by linked read haplotyping and Bayesian approach.

Noninvasive prenatal diagnosis of genetic diseases induced by triplet repeat expansion by linked read haplotyping and Bayesian approach.

Journal: Scientific reports

Published: January 07, 2022

Robust Detection of Somatic Mosaicism and Repeat Interruptions by Long-Read Targeted Sequencing in Myotonic Dystrophy Type 1.

Robust Detection of Somatic Mosaicism and Repeat Interruptions by Long-Read Targeted Sequencing in Myotonic Dystrophy Type 1.

Journal: International journal of molecular sciences

Published: February 12, 2021

Single Circulating Fetal Trophoblastic Cells Eligible for Non Invasive Prenatal Diagnosis: the Exception Rather than the Rule.

Single Circulating Fetal Trophoblastic Cells Eligible for Non Invasive Prenatal Diagnosis: the Exception Rather than the Rule.

Journal: Scientific reports

Published: January 28, 2020

Male partners of infertile couples with congenital unilateral absence of the vas deferens are mainly non-azoospermic.

Male partners of infertile couples with congenital unilateral absence of the vas deferens are mainly non-azoospermic.

Journal: Andrology

Published: August 14, 2019

Linear lesions: A key dermatological feature of X-linked ectodermal dysplasia in a young girl

Linear lesions: A key dermatological feature of X-linked ectodermal dysplasia in a young girl

Journal: Annales de dermatologie et de venereologie

Published: January 31, 2019

Evaluation of the template letter regarding the disclosure of genetic information within the family in France.

Evaluation of the template letter regarding the disclosure of genetic information within the family in France.

Journal: Journal of community genetics

Published: March 30, 2018

Sperm aneuploidy and DNA fragmentation in unexplained recurrent pregnancy loss: a multicenter case-control study.

Sperm aneuploidy and DNA fragmentation in unexplained recurrent pregnancy loss: a multicenter case-control study.

Journal: Basic and clinical andrology

Published: January 18, 2018

Clinical and evolutionary characteristics of a child with aquagenic keratoderma: A retrospective study of 12 patients

Clinical and evolutionary characteristics of a child with aquagenic keratoderma: A retrospective study of 12 patients

Journal: Annales de dermatologie et de venereologie

Published: May 18, 2017

Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens.

Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens.

Journal: American journal of human genetics

Published: February 18, 2016

The spectrum of renal involvement in male patients with infertility related to excretory-system abnormalities: phenotypes, genotypes, and genetic counseling.

The spectrum of renal involvement in male patients with infertility related to excretory-system abnormalities: phenotypes, genotypes, and genetic counseling.

Journal: Journal of nephrology

Published: December 09, 2015

Showing 1-11 of 11

Last Updated: 09/26/2026