Publications by authors named "Sophie Dahoun"

32Publications

Observational study of disorders of sex development in Yaounde, Cameroon.

J Pediatr Endocrinol Metab 2020 Mar;33(3):417-423

Mother and Child Center of the Chantal Biya Foundation Yaounde, Faculty of Medicine and Biomedical Sciences, Department of Paediatrics, Yaounde, Cameroon.

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http://dx.doi.org/10.1515/jpem-2019-0458DOI Listing
March 2020

MECP2 duplication syndrome in a patient from Cameroon.

Am J Med Genet A 2020 04 13;182(4):619-622. Epub 2020 Feb 13.

Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

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http://dx.doi.org/10.1002/ajmg.a.61510DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450984PMC
April 2020

The 22q11.2 Deletion Syndrome in Congenital Heart Defects: Prevalence of Microdeletion Syndrome in Cameroon.

Glob Heart 2017 06 13;12(2):115-120. Epub 2017 Mar 13.

Service of Genetic Medicine, Geneva University Hospitals, Geneva, Switzerland.

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http://dx.doi.org/10.1016/j.gheart.2017.01.003DOI Listing
June 2017

Laparoscopic-assisted vaginal pull-through: A new approach for congenital adrenal hyperplasia patients with high urogenital sinus.

Afr J Paediatr Surg 2015 Jul-Sep;12(3):177-80

Department of Paediatric Surgery, University Claude Bernard Lyon 1, Hôpital Femme Mère Enfant, 69677 Bron Cedex, France.

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http://dx.doi.org/10.4103/0189-6725.170191DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955429PMC
December 2016

Challenges in clinical diagnosis of williams-beuren syndrome in sub-saharan africans: case reports from cameroon.

Mol Syndromol 2014 Dec 29;5(6):287-92. Epub 2014 Nov 29.

Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon ; Division of Human Genetics, University of Cape Town, Cape Town, South Africa.

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http://dx.doi.org/10.1159/000369421DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4281575PMC
December 2014

A novel SRY mutation leads to asymmetric SOX9 activation and is responsible for mixed 46,XY gonadal dysgenesis.

Horm Res Paediatr 2012 22;78(3):188-92. Epub 2012 Mar 22.

Endocrine and Diabetes Unit, Department of Pediatrics, University Hospital of Geneva, Geneva, Switzerland.

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http://dx.doi.org/10.1159/000336925DOI Listing
May 2013

Preliminary structure and predictive value of attenuated negative symptoms in 22q11.2 deletion syndrome.

Psychiatry Res 2012 Apr 27;196(2-3):277-84. Epub 2012 Feb 27.

Department of Psychiatry, University of Geneva School of Medicine, Geneva, Switzerland.

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http://dx.doi.org/10.1016/j.psychres.2011.08.017DOI Listing
April 2012

Initiation of prenatal genetic diagnosis of chromosomal anomalies in Cameroon.

Int J Gynaecol Obstet 2012 Feb 9;116(2):174-5. Epub 2011 Nov 9.

Faculty of Medicine and Biomedical Sciences, University of Yaoundé, Yaoundé Cameroon.

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http://dx.doi.org/10.1016/j.ijgo.2011.10.006DOI Listing
February 2012

Down syndrome: parental origin, recombination, and maternal age.

Genet Test Mol Biomarkers 2012 Jan 23;16(1):70-3. Epub 2011 Aug 23.

Department of Biology and Medical Genetics, School of Medicine, University of Rijeka, Rijeka, Croatia.

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http://dx.doi.org/10.1089/gtmb.2011.0066DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265771PMC
January 2012

Initiation of a medical genetics service in sub-Saharan Africa: experience of prenatal diagnosis in Cameroon.

Eur J Med Genet 2011 Jul-Aug;54(4):e399-404. Epub 2011 Apr 5.

Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Cameroon.

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http://dx.doi.org/10.1016/j.ejmg.2011.03.013DOI Listing
October 2011

Derivation of the first Swiss human embryonic stem cell line from a single blastomere of an arrested four-cell stage embryo.

Swiss Med Wkly 2008 Sep;138(37-38):540-50

Laboratory of Stem Cell Research, Department of Obstetrics and Gynaecology, Geneva University Hospitals, Geneva, Switzerland.

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http://dx.doi.org/2008/37/smw-12385DOI Listing
September 2008

A de novo 1.1-1.6 Mb subtelomeric deletion of chromosome 20q13.33 in a patient with learning difficulties but without obvious dysmorphic features.

Am J Med Genet A 2007 Aug;143A(16):1894-9

Service of Medical Genetics, Department of Gynecology and Obstetrics, Geneva University Hospitals, Geneva, Switzerland.

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http://dx.doi.org/10.1002/ajmg.a.31789DOI Listing
August 2007

Mechanisms regulating the proliferative potential of human CD8+ T lymphocytes overexpressing telomerase.

J Immunol 2006 Sep;177(6):3657-68

National Center of Competence in Research Molecular Oncology, Swiss Institute for Experimental Cancer Research, Epalinges, Switzerland.

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http://dx.doi.org/10.4049/jimmunol.177.6.3657DOI Listing
September 2006

No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome.

Am J Psychiatry 2006 Mar;163(3):537-9

Department of Genetic Medicine, University of Geneva Medical School and University Hospitals, Switzerland.

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http://dx.doi.org/10.1176/appi.ajp.163.3.537DOI Listing
March 2006

Establishment of permanent cell lines purified from human mesothelioma: morphological aspects, new marker expression and karyotypic analysis.

Histochem Cell Biol 2004 Sep 15;122(3):249-60. Epub 2004 Sep 15.

Department of Thoracic Surgery, Cantonal Hospital of Geneva University, 1, rue Micheli-du-Crest, 1211, 4, Switzerland.

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http://dx.doi.org/10.1007/s00418-004-0701-1DOI Listing
September 2004

Parental decisions following the prenatal diagnosis of sex chromosome abnormalities.

Eur J Obstet Gynecol Reprod Biol 2004 Sep;116(1):58-62

Laboratoire de Cytogénétique, Division de Génétique Médicale, CMU, 1 rue Michel Servet, 1211 Genève 4, Switzerland.

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http://linkinghub.elsevier.com/retrieve/pii/S030121150400081
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http://dx.doi.org/10.1016/j.ejogrb.2003.12.029DOI Listing
September 2004

No association between DUP25 and anxiety disorders.

Am J Med Genet B Neuropsychiatr Genet 2004 Jul;128B(1):80-3

Division de Génétique Médicale, Hôpitaux Universitaires de Genève, 1 rue Michel Servet 1211, Geneva 4, Switzerland.

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http://doi.wiley.com/10.1002/ajmg.b.30037
Publisher Site
http://dx.doi.org/10.1002/ajmg.b.30037DOI Listing
July 2004

[Anomalies of sex chromosomes in amniocentesis].

Rev Med Suisse Romande 2004 Mar;124(3):167-9

Division de Génétique Médicale Hôpitoux Universitaires de Genève.

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March 2004

Turner syndrome with complex mosaic monosomy and structural aorta anomalies.

J Pediatr 2003 Mar;142(3):341

Pediatric Cardiology Unit Division of Radiology Division of Medical Genetics Hôpitaux Universitaires de Genève Geneva, Switzerland.

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http://dx.doi.org/10.1067/mpd.2003.29DOI Listing
March 2003

Is genetic analysis useful in the routine management of hydatidiform mole?

Hum Reprod 2003 Feb;18(2):243-9

Department of Gynecology and Obstetrics, University Hospitals of Geneva, Boulevard de la Cluse 30, 1211 Geneva 14, Switzerland.

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http://dx.doi.org/10.1093/humrep/deg091DOI Listing
February 2003

Language skills in children with velocardiofacial syndrome (deletion 22q11.2).

J Pediatr 2002 Jun;140(6):753-8

Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, California, USA.

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http://dx.doi.org/10.1067/mpd.2002.124774DOI Listing
June 2002