A comprehensive clinical and genetic study in 127 patients with ID in Kinshasa, DR Congo

Author:

Lumaka Aimé1234ORCID,Race Valerie5,Peeters Hilde5,Corveleyn Anniek5,Coban‐Akdemir Zeynep6,Jhangiani Shalini N.6,Song Xiaofei6,Mubungu Gerrye1345ORCID,Posey Jennifer7,Lupski James R.6789,Vermeesch Joris R.5,Lukusa Prosper1235ORCID,Devriendt Koenraad5

Affiliation:

1. Centre for Human Genetics, Faculty of MedicineUniversity of Kinshasa Kinshasa DR Congo

2. Département des Sciences Biomédicales et Précliniques, GIGA‐RLaboratoire de Génétique Humaine, University of Liège Liège Belgium

3. Institut National de Recherche Biomédicale Kinshasa DR Congo

4. Department of Pediatrics, Faculty of MedicineUniversity of Kinshasa Kinshasa DR Congo

5. Centre for Human Genetics, University HospitalUniversity of Leuven Leuven Belgium

6. Department of Molecular and Human GeneticsBaylor College of Medicine Houston Texas

7. Human Genome Sequencing CenterBaylor College of Medicine Houston Texas

8. Department of PediatricsBaylor College of Medicine Houston Texas

9. Genetics Clinic service, Texas Children's Hospital Houston Texas

Funder

Fonds Wetenschappelijk Onderzoek

National Human Genome Research Institute

KU Leuven

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference72 articles.

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3. An experimental loop design for the detection of constitutional chromosomal aberrations by array CGH

4. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen‐receptor gene correlates with X chromosome inactivation;Allen R. C.;American Journal of Human Genetics,1992

5. X Chromosome–Inactivation Patterns of 1,005 Phenotypically Unaffected Females

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