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Publications by Danièle Depétris

Interstitial 22q11 Microdeletion Excluding the ADU Breakpoint in a Patient With DiGeorge Syndrome

Human Molecular Genetics

Molecular Biology

English

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A Novel 22q11.2 Microdeletion in DiGeorge Syndrome

American Journal of Human Genetics

English

P01.02: Frequency of 22q11 Microdeletion Syndrome in Fetuses With Conotruncal Heart Disease

Ultrasound in Obstetrics and Gynecology

Nuclear Medicine

Ultrasound Technology

Reproductive Medicine

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Recurrence of DiGeorge Syndrome: Prenatal Detection by FISH of a Molecular 22q11 Deletion.

Journal of Medical Genetics

English

Der(22) Syndrome and Velo-Cardio-Facial Syndrome/DiGeorge Syndrome Share a 1.5-Mb Region of Overlap on Chromosome 22q11

American Journal of Human Genetics

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805 IN SITU HYBRIDIZATION AND TRANSLOCATION BREAKPOINT (DGS) MAPPING III. DiGEORGE SYNDROME (DGS) WITH PARTIAL MONOSOMY OF CHROMOSOME 22

Pediatric Research

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Successful T-Cell Reconstitution After Unrelated Cord Blood Transplantation in a Patient With Complete DiGeorge Syndrome

Journal of Allergy and Clinical Immunology

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Y Chromosome Microdeletion in a Case With Klinefelter's Syndrome

Archives of Andrology

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3q29 Microdeletion Syndrome

English

3q13 Microdeletion Syndrome

English