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

Human Molecular Genetics - United Kingdom
doi 10.1093/hmg/4.12.2417
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Oxford University Press (OUP)

Related search

A Novel 22q11.2 Microdeletion in DiGeorge Syndrome

American Journal of Human Genetics
Genetics
1999English

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

Ultrasound in Obstetrics and Gynecology
Nuclear MedicineRadiologyUltrasound TechnologyGynecologyReproductive MedicineRadiologicalImagingObstetricsMedicine
2018English

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

Journal of Medical Genetics
Genetics
1995English

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
Genetics
1999English

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

Pediatric Research
Child HealthPediatricsPerinatology
1985English

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

Journal of Allergy and Clinical Immunology
AllergyImmunology
2016English

Y Chromosome Microdeletion in a Case With Klinefelter's Syndrome

Archives of Andrology
2006English

3q29 Microdeletion Syndrome

2020English

3q13 Microdeletion Syndrome

2020English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy