2015

Scientific Articles

unige:83732

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

Birraux, Jacques Maurice; Mouafo, Faustin Tambo; Dahoun, Sophie; Tardy, Veronique; ... Mure, Pierre-Yves

2014

Scientific Articles

unige:34274

Modelling and rescuing neurodevelopmental defect of Down syndrome using induced pluripotent stem cells from monozygotic twins discordant for trisomy 21

Hibaoui, Youssef; Grad, Iwona; Letourneau, Audrey; Sailani, Mohammad Reza; ... Feki, Anis

2013

Scientific Articles

unige:29136

Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes

Delio, Maria; Schneider, Maude; Dahoun, Sophie; Eliez, Stéphan; Armando, Marco

Privat-docent Thesis

unige:26598

Evolution des indications des diagnostics prénatals de 1999 à 2011 suite à l’introduction du test combiné à Genève

Dahoun, Sophie;

2012

Scientific Articles

unige:27579	A novel SRY mutation leads to asymmetric SOX9 activation and is responsible for mixed 46,XY gonadal dysgenesis	Klee, Philippe; Bena, Frédérique; Birraux, Jacques Maurice; Dahoun, Sophie; ... Schwitzgebel Luscher, Valérie
unige:34656	Homozygous deletion of a gene-free region of 4p15 in a child with multiple anomalies: could biallelic loss of conserved, non-coding elements lead to a phenotype?	Makrythanasis, Periklis; Gimelli, Stefania; Sloan Bena, Frédérique; Dahoun, Sophie; ... Bottani, Armand
unige:29126	Preliminary structure and predictive value of attenuated negative symptoms in 22q11.2 deletion syndrome	Schneider, Maude; Van der Linden, Martial; Glaser, Bronwyn; Rizzi, Eleonora; ... Eliez, Stéphan

2011

Scientific Articles

unige:32205	Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report	Antonarakis, Stylianos; Fokstuen, Siv; Engel, Eric; Dermitzakis, Emmanouil; ... Mostafavi, Maryam
unige:25159	NANOG priming before full reprogramming may generate germ cell tumours	Grad, Iwona; Hibaoui, Youssef; Jaconi, Marisa; Chicha, Laurie; ... Feki, Anis

2009

Scientific Articles

unige:5576

Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21

Lyle, Robert; Bena, Frédérique; Gagos, Sarantis; Gehrig, Corinne; ... Antonarakis, Stylianos

2008

Scientific Articles

unige:1441	Derivation of the first Swiss human embryonic stem cell line from a single blastomere of an arrested four-cell stage embryo	Feki, Anis; Bosman, Alexis; Dubuisson, Jean-Bernard; Irion, Olivier; ... Jaconi, Marisa
unige:1188	Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: a complex series of events	Dahoun, Sophie; Gagos, Sarantis; Gagnebin, Maryline; Gehrig, Corinne; ... Blouin, Jean-Louis
unige:8884	Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients	Martinet, Danielle; Filges, Isabel; Besuchet Schmutz, Nathalie; Morris, Michael Andréw; ... Bena, Frédérique
unige:1796	Unusually stable abnormal karyotype in a highly aggressive melanoma negative for telomerase activity	Gagos, Sarantis; Papaioannou, George; Chiourea, Maria; Merk-Loretti, Sophie; ... Dahoun, Sophie

2007

Scientific Articles

unige:8871

Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21

Lyle, Robert; Prandini, Paola; Osoegawa, Kazutoyo; ten Hallers, Boudewijn; ... Antonarakis, Stylianos

2006

Scientific Articles

unige:5369

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

Glaser, Bronwyn; Debbané, Martin; Hinard, Christine; Morris, Michael Andréw; ... Eliez, Stéphan

2004

Scientific Articles

unige:41987	Establishment of permanent cell lines purified from human mesothelioma: morphological aspects, new marker expression and karyotypic analysis	Philippeaux, Marie-Marthe; Pache, Jean-Claude; Dahoun, Sophie; Barnet, Marc; ... Spiliopoulos, Anastase
unige:8802	No association between DUP25 and anxiety disorders	Henrichsen, C. N.; Delorme, Richard; Boucherie, Maria; Marelli, Dominique; ... Dahoun, Sophie

2003

Scientific Articles

unige:55250

Turner syndrome with complex mosaic monosomy and structural aorta anomalies

Tissières, Pierre; Didier, Dominique; Dahoun, Sophie; Jaeggi, Edgard;

2000

Scientific Articles

unige:73171

A case of 45,X Turner syndrome with spontaneous ovulation proven by ultrasonography

Giacobino, Ariane; Dahoun, Sophie; Sizonenko, Pierre-Claude; Stalberg, Anna-Maria; ... Campana, Aldo