Cedric Le Caignec

Cedric Le Caignec

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Cedric Le Caignec

Publications by authors named "Cedric Le Caignec"

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Whole genome paired-end sequencing elucidates functional and phenotypic consequences of balanced chromosomal rearrangement in patients with developmental disorders.

J Med Genet 2019 Aug 28;56(8):526-535. Epub 2019 Mar 28.

Service de Génétique, Hospices Civils de Lyon, Bron, France.

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http://dx.doi.org/10.1136/jmedgenet-2018-105778DOI Listing
August 2019

Clinical, Histopathological, and Molecular Diagnostics in Lethal Lung Developmental Disorders.

Am J Respir Crit Care Med 2019 Jun 12. Epub 2019 Jun 12.

Baylor College of Medicine, Department of Molecular & Human Genetics, Houston , Texas, United States ;

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http://dx.doi.org/10.1164/rccm.201903-0495TRDOI Listing
June 2019

Oro-dental phenotype in patients with RUNX2 duplication.

Eur J Med Genet 2019 Feb 29;62(2):85-89. Epub 2018 May 29.

Service d'Odontologie Conservatrice et Pédiatrique, Centre de compétences Malformations orales et dentaires rares, CHU de Nantes, France; Département D'Odontologie Pédiatrique, UFR Odontologie, Université de Nantes, France; Unité d'Investigation Clinique Odontologie (UIC), France. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2018.05.019DOI Listing
February 2019

Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF Pathway.

Am J Hum Genet 2019 Feb 10;104(2):213-228. Epub 2019 Jan 10.

Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Baylor Genetics, Houston, TX 77021, USA; Institute of Mother and Child, 01-211 Warsaw, Poland. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00029297183046
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http://dx.doi.org/10.1016/j.ajhg.2018.12.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369446PMC
February 2019

A de novo 2q37.2 deletion encompassing AGAP1 and SH3BP4 in a patient with autism and intellectual disability.

Eur J Med Genet 2018 Nov 22. Epub 2018 Nov 22.

CHU Nantes, Service de Génétique Médicale, Nantes, France; INSERM, UMR 1238, Bone Sarcoma and Remodeling of Calcified Tissue, Nantes, France.

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http://dx.doi.org/10.1016/j.ejmg.2018.11.020DOI Listing
November 2018

Familial autosomal dominant severe ankyloglossia with tooth abnormalities.

Am J Med Genet A 2018 07 28;176(7):1614-1617. Epub 2018 Apr 28.

Service de Génétique Médicale, CHU de Nantes, Nantes, France.

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http://dx.doi.org/10.1002/ajmg.a.38690DOI Listing
July 2018

Further delineation of the duplication syndrome phenotype in 59 French male patients, with a particular focus on morphological and neurological features.

Authors:
Marguerite Miguet Laurence Faivre Jeanne Amiel Mathilde Nizon Renaud Touraine Fabienne Prieur Laurent Pasquier Mathilde Lefebvre Julien Thevenon Christèle Dubourg Sophie Julia Catherine Sarret Ganaëlle Remerand Christine Francannet Fanny Laffargue Odile Boespflug-Tanguy Albert David Bertrand Isidor Jacqueline Vigneron Bruno Leheup Laetitia Lambert Christophe Philippe Mylène Béri-Dexheimer Jean-Marie Cuisset Joris Andrieux Ghislaine Plessis Annick Toutain Laurent Guibaud Valérie Cormier-Daire Marlene Rio Jean-Paul Bonnefont Bernard Echenne Hubert Journel Lydie Burglen Sandrine Chantot-Bastaraud Thierry Bienvenu Clarisse Baumann Laurence Perrin Séverine Drunat Pierre-Simon Jouk Klaus Dieterich Françoise Devillard Didier Lacombe Nicole Philip Sabine Sigaudy Anne Moncla Chantal Missirian Catherine Badens Nathalie Perreton Christel Thauvin-Robinet Réseau AChro-Puce Jean-Michel Pedespan Caroline Rooryck Cyril Goizet Catherine Vincent-Delorme Bénédicte Duban-Bedu Nadia Bahi-Buisson Alexandra Afenjar Kim Maincent Delphine Héron Jean-Luc Alessandri Dominique Martin-Coignard Gaëtan Lesca Massimiliano Rossi Martine Raynaud Patrick Callier Anne-Laure Mosca-Boidron Nathalie Marle Charles Coutton Véronique Satre Cédric Le Caignec Valérie Malan Serge Romana Boris Keren Anne-Claude Tabet Valérie Kremer Sophie Scheidecker Adeline Vigouroux Marilyn Lackmy-Port-Lis Damien Sanlaville Marianne Till Maryline Carneiro Brigitte Gilbert-Dussardier Marjolaine Willems Hilde Van Esch Vincent Des Portes Salima El Chehadeh

J Med Genet 2018 Jun 4;55(6):359-371. Epub 2018 Apr 4.

Service de génétique médicale, Institut de Génétique Médicale d'Alsace (IGMA), Centre de Référence Maladies Rares "Anomalies du développement et syndromes malformatifs", Centre de Référence Maladies Rares "Des déficiences intellectuelles de causes rares", Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, Strasbourg, France.

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http://dx.doi.org/10.1136/jmedgenet-2017-104956DOI Listing
June 2018

Comparison of Tumor- and Bone Marrow-Derived Mesenchymal Stromal/Stem Cells from Patients with High-Grade Osteosarcoma.

Int J Mol Sci 2018 Mar 1;19(3). Epub 2018 Mar 1.

Laboratoire d'étude des sarcomes osseux et remodelage des tissus calcifiés, INSERM UMR 1238, Université de Nantes, PhyOS, 44034 Nantes CEDEX 1, France.

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http://dx.doi.org/10.3390/ijms19030707DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5877568PMC
March 2018

Copy Number Variations Found in Patients with a Corpus Callosum Abnormality and Intellectual Disability.

J Pediatr 2017 06 8;185:160-166.e1. Epub 2017 Mar 8.

APHP, GH Pitié Salpêtrière, Department of genetics, unit of medical genetics, reference center for intellectual disabilities of rare causes, Paris, France; GRC Intellectual Disability and Autism, UPMC, Paris, France; Sorbonne Universités, UPMC Univ Paris 06, UMR S 1127, Inserm U 1127, CNRS UMR 7225, ICM, Paris, France; APHP, Hôpital Armand-Trousseau, Department of genetics, Division of clinical genetics, Paris, France.

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http://dx.doi.org/10.1016/j.jpeds.2017.02.023DOI Listing
June 2017

Mandibular dysostosis without microphthalmia caused by OTX2 deletion.

Am J Med Genet A 2016 09 5;170(9):2466-70. Epub 2016 Jul 5.

Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France.

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http://dx.doi.org/10.1002/ajmg.a.37837DOI Listing
September 2016

Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.

Am J Hum Genet 2016 09 25;99(3):540-554. Epub 2016 Aug 25.

Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA; Center for Autism Research and Treatment and Program in Neurobehavioral Genetics, Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA 90095, USA; Department of Human Genetics, University of California, Los Angeles, Los Angeles, CA 90095, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2016.06.036DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011063PMC
September 2016

Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations.

Orphanet J Rare Dis 2015 Oct 15;10:135. Epub 2015 Oct 15.

CHU Nantes, Service de Génétique Médicale, Unité de Génétique Moléculaire, 9 quai Moncousu, 44093, Nantes CEDEX 1, France.

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http://link.springer.com/content/pdf/10.1186%2Fs13023-015-03
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http://www.ojrd.com/content/10/1/135
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http://dx.doi.org/10.1186/s13023-015-0352-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608180PMC
October 2015

Patients with isolated oligo/hypodontia caused by RUNX2 duplication.

Am J Med Genet A 2015 Jun 21;167(6):1386-90. Epub 2015 Apr 21.

CHU Nantes, Service de Génétique Médicale, Nantes, France.

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http://dx.doi.org/10.1002/ajmg.a.37052DOI Listing
June 2015

Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disability.

Eur J Hum Genet 2015 May 30;23(5):628-32. Epub 2014 Jul 30.

Center for Medical Genetics, Ghent University, Ghent University Hospital, Ghent, Belgium.

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http://dx.doi.org/10.1038/ejhg.2014.141DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4402620PMC
May 2015

A de novo ADCY5 mutation causes early-onset autosomal dominant chorea and dystonia.

Mov Disord 2015 Mar 27;30(3):423-7. Epub 2014 Dec 27.

Plateforme GENOMAX, Laboratoire d'ImmunoRhumatologie Moléculaire, INSERM UMR_S1109, Centre de Recherche d'Immunologie et d'Hématologie, Faculté de Médecine, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg, Strasbourg, France.

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http://dx.doi.org/10.1002/mds.26115DOI Listing
March 2015

Disruption of the SEMA3D gene in a patient with congenital heart defects.

Hum Mutat 2015 Jan 28;36(1):30-3. Epub 2014 Nov 28.

INSERM, UMR1087, l'institut du thorax, Nantes, France; Université de Nantes, Nantes, France.

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http://dx.doi.org/10.1002/humu.22702DOI Listing
January 2015

[Extra-oral signs to look for in patients exhibiting oral warning signs of genetic diseases].

C R Biol 2015 Jan 4;338(1):48-57. Epub 2014 Nov 4.

Département d'odontologie pédiatrique, faculté de chirurgie dentaire de Nantes, 44042 Nantes cedex 01, France; Service d'odontologie conservatrice et pédiatrique, CHU de Nantes, 44000 Nantes, France.

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http://dx.doi.org/10.1016/j.crvi.2014.10.001DOI Listing
January 2015

An emerging phenotype of Xq22 microdeletions in females with severe intellectual disability, hypotonia and behavioral abnormalities.

J Hum Genet 2014 Jun 20;59(6):300-6. Epub 2014 Mar 20.

1] Department of Clinical Genetics, Sahlgrenska University Hospital, Gothenburg, Sweden [2] Department of Medical and Clinical Genetics, Sahlgrenska Academy, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden [3] Department of Clinical Genetics, University Hospital Linköping, Linköping, Sweden.

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http://dx.doi.org/10.1038/jhg.2014.21DOI Listing
June 2014

Mutations in FAM111B cause hereditary fibrosing poikiloderma with tendon contracture, myopathy, and pulmonary fibrosis.

Am J Hum Genet 2013 Dec 21;93(6):1100-7. Epub 2013 Nov 21.

Unité de Génétique Clinique, Service de Génétique Médicale, Centre de Référence Anomalies de Développement et Syndromes Malformatifs de l'Interrégion Grand-Ouest, Centre Hospitalier Universitaire Nantes, 9 Quai Moncousu, 44093 Nantes Cedex 1, France; Institut National de la Santé et de la Recherche Médicale UMR 1089, Atlantic Gene Therapy Institute, University of Nantes, 44007 Nantes, France.

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http://dx.doi.org/10.1016/j.ajhg.2013.10.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853004PMC
December 2013

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations.

Nephron Physiol 2012 23;122(1-2):1-6. Epub 2013 Feb 23.

Centre for Nephrology, University College London, London, UK.

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http://dx.doi.org/10.1159/000349989DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782194PMC
October 2013

A new form of severe spondyloepimetaphyseal dysplasia: clinical and radiological characterization.

Am J Med Genet A 2013 Oct 16;161A(10):2645-51. Epub 2013 Aug 16.

Service de Génétique Médicale, CHU de Nantes, Nantes, France; INSERM, UMR-S 957, Nantes, France.

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http://dx.doi.org/10.1002/ajmg.a.36132DOI Listing
October 2013

Constitutional telomeric association (Y;7) in a patient with a female phenotype.

Am J Med Genet A 2013 Jun 23;161A(6):1436-41. Epub 2013 Apr 23.

CHU Nantes, Service de Génétique Médicale, Nantes, France.

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http://dx.doi.org/10.1002/ajmg.a.35889DOI Listing
June 2013

Autosomal insertional translocation mimicking an X-linked mode of inheritance.

Eur J Med Genet 2013 Jan 26;56(1):46-9. Epub 2012 Oct 26.

CHU Nantes, Service de Génétique Médicale, 9 quai Moncousu, 44093 Nantes, France.

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http://dx.doi.org/10.1016/j.ejmg.2012.10.006DOI Listing
January 2013

De novo duplication and deletions at 7q in a three-generation family.

Am J Med Genet A 2012 Jun 10;158A(6):1493-7. Epub 2012 May 10.

CHU de Nantes, Service de Génétique Médicale, Nantes, France.

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http://dx.doi.org/10.1002/ajmg.a.35332DOI Listing
June 2012

Barth syndrome in a female patient.

Mol Genet Metab 2012 May 24;106(1):115-20. Epub 2012 Jan 24.

Service de Médecine Pédiatrique, CHRU de Tours, Université François Rabelais, Tours, France.

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https://linkinghub.elsevier.com/retrieve/pii/S10967192120001
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http://dx.doi.org/10.1016/j.ymgme.2012.01.015DOI Listing
May 2012

Serpentine fibula-polycystic kidney syndrome caused by truncating mutations in NOTCH2.

Hum Mutat 2011 Nov 12;32(11):1239-42. Epub 2011 Sep 12.

CHU Nantes, Service de Génétique Médicale, Nantes, France.

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http://dx.doi.org/10.1002/humu.21563DOI Listing
November 2011

[Human diseases and NOTCH receptors].

Med Sci (Paris) 2011 Jun-Jul;27(6-7):593-5. Epub 2011 Jul 1.

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http://dx.doi.org/10.1051/medsci/2011276011DOI Listing
September 2011

Five patients with novel overlapping interstitial deletions in 8q22.2q22.3.

Am J Med Genet A 2011 Aug 7;155A(8):1857-64. Epub 2011 Jul 7.

Institut für Humangenetik, Universitätsklinikum Essen, Essen, Germany.

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http://dx.doi.org/10.1002/ajmg.a.34072DOI Listing
August 2011

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.

Authors:
Sébastien Jacquemont Alexandre Reymond Flore Zufferey Louise Harewood Robin G Walters Zoltán Kutalik Danielle Martinet Yiping Shen Armand Valsesia Noam D Beckmann Gudmar Thorleifsson Marco Belfiore Sonia Bouquillon Dominique Campion Nicole de Leeuw Bert B A de Vries Tõnu Esko Bridget A Fernandez Fernando Fernández-Aranda José Manuel Fernández-Real Mònica Gratacòs Audrey Guilmatre Juliane Hoyer Marjo-Riitta Jarvelin R Frank Kooy Ants Kurg Cédric Le Caignec Katrin Männik Orah S Platt Damien Sanlaville Mieke M Van Haelst Sergi Villatoro Gomez Faida Walha Bai-Lin Wu Yongguo Yu Azzedine Aboura Marie-Claude Addor Yves Alembik Stylianos E Antonarakis Benoît Arveiler Magalie Barth Nathalie Bednarek Frédérique Béna Sven Bergmann Mylène Beri Laura Bernardini Bettina Blaumeiser Dominique Bonneau Armand Bottani Odile Boute Han G Brunner Dorothée Cailley Patrick Callier Jean Chiesa Jacqueline Chrast Lachlan Coin Charles Coutton Jean-Marie Cuisset Jean-Christophe Cuvellier Albert David Bénédicte de Freminville Bruno Delobel Marie-Ange Delrue Bénédicte Demeer Dominique Descamps Gérard Didelot Klaus Dieterich Vittoria Disciglio Martine Doco-Fenzy Séverine Drunat Bénédicte Duban-Bedu Christèle Dubourg Julia S El-Sayed Moustafa Paul Elliott Brigitte H W Faas Laurence Faivre Anne Faudet Florence Fellmann Alessandra Ferrarini Richard Fisher Elisabeth Flori Lukas Forer Dominique Gaillard Marion Gerard Christian Gieger Stefania Gimelli Giorgio Gimelli Hans J Grabe Agnès Guichet Olivier Guillin Anna-Liisa Hartikainen Délphine Heron Loyse Hippolyte Muriel Holder Georg Homuth Bertrand Isidor Sylvie Jaillard Zdenek Jaros Susana Jiménez-Murcia Géraldine Joly Helas Philippe Jonveaux Satu Kaksonen Boris Keren Anita Kloss-Brandstätter Nine V A M Knoers David A Koolen Peter M Kroisel Florian Kronenberg Audrey Labalme Emilie Landais Elisabetta Lapi Valérie Layet Solenn Legallic Bruno Leheup Barbara Leube Suzanne Lewis Josette Lucas Kay D MacDermot Pall Magnusson Christian Marshall Michèle Mathieu-Dramard Mark I McCarthy Thomas Meitinger Maria Antonietta Mencarelli Giuseppe Merla Alexandre Moerman Vincent Mooser Fanny Morice-Picard Mafalda Mucciolo Matthias Nauck Ndeye Coumba Ndiaye Ann Nordgren Laurent Pasquier Florence Petit Rolph Pfundt Ghislaine Plessis Evica Rajcan-Separovic Gian Paolo Ramelli Anita Rauch Roberto Ravazzolo Andre Reis Alessandra Renieri Cristobal Richart Janina S Ried Claudine Rieubland Wendy Roberts Katharina M Roetzer Caroline Rooryck Massimiliano Rossi Evald Saemundsen Véronique Satre Claudia Schurmann Engilbert Sigurdsson Dimitri J Stavropoulos Hreinn Stefansson Carola Tengström Unnur Thorsteinsdóttir Francisco J Tinahones Renaud Touraine Louis Vallée Ellen van Binsbergen Nathalie Van der Aa Catherine Vincent-Delorme Sophie Visvikis-Siest Peter Vollenweider Henry Völzke Anneke T Vulto-van Silfhout Gérard Waeber Carina Wallgren-Pettersson Robert M Witwicki Simon Zwolinksi Joris Andrieux Xavier Estivill James F Gusella Omar Gustafsson Andres Metspalu Stephen W Scherer Kari Stefansson Alexandra I F Blakemore Jacques S Beckmann Philippe Froguel

Nature 2011 Aug 31;478(7367):97-102. Epub 2011 Aug 31.

Service of Medical Genetics, Centre Hospitalier Universitaire Vaudois, 1011 Lausanne, Switzerland.

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http://dx.doi.org/10.1038/nature10406DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3637175PMC
August 2011

Homozygous PTEN deletion in neuroblastoma arising in a child with Cowden syndrome.

Am J Med Genet A 2011 Jul 10;155A(7):1763-6. Epub 2011 Jun 10.

CHU Nantes, service d'hemato-oncologie pédiatrique, France.

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http://dx.doi.org/10.1002/ajmg.a.34066DOI Listing
July 2011

Oligonucleotide microarrays in constitutional genetic diagnosis.

Expert Rev Mol Diagn 2011 Jun;11(5):521-32

Groupe Hospitalier Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, Département de Génétique et Cytogénétique, France.

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http://dx.doi.org/10.1586/erm.11.32DOI Listing
June 2011

A new microdeletion syndrome of 5q31.3 characterized by severe developmental delays, distinctive facial features, and delayed myelination.

Am J Med Genet A 2011 Apr 15;155A(4):732-6. Epub 2011 Mar 15.

Tokyo Women's Medical University Institute for Integrated Medical Sciences, Tokyo, Japan.

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http://dx.doi.org/10.1002/ajmg.a.33891DOI Listing
April 2011

Mesomelic dysplasia Kantaputra type is associated with duplications of the HOXD locus on chromosome 2q.

Eur J Hum Genet 2010 Dec 21;18(12):1310-4. Epub 2010 Jul 21.

Department of Pediatric Dentistry, Craniofacial Genetics Laboratory, Faculty of Dentistry, Chiang Mai University, Chiang Mai, Thailand.

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http://dx.doi.org/10.1038/ejhg.2010.116DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002849PMC
December 2010

Deletion of the CUL4B gene in a boy with mental retardation, minor facial anomalies, short stature, hypogonadism, and ataxia.

Am J Med Genet A 2010 Jan;152A(1):175-80

Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes 7, Quai Moncousu, 44000 Nantes Cedex, France.

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http://dx.doi.org/10.1002/ajmg.a.33152DOI Listing
January 2010

Copy number variation goes clinical.

Genome Biol 2009 23;10(1):301. Epub 2009 Jan 23.

CHU de Nantes, Service de Génétique Médicale, Nantes, France.

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http://dx.doi.org/10.1186/gb-2009-10-1-301DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2687785PMC
September 2009

Three independent mutations in the TSC2 gene in a family with tuberous sclerosis.

Eur J Hum Genet 2009 Sep 4;17(9):1165-70. Epub 2009 Mar 4.

Centre Hospitalier Universitaire de Nantes, Service de Génétique Médicale, Nantes, France.

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http://dx.doi.org/10.1038/ejhg.2009.28DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874752PMC
September 2009

Familial frameshift SRY mutation inherited from a mosaic father with testicular dysgenesis syndrome.

J Clin Endocrinol Metab 2009 Sep 16;94(9):3467-71. Epub 2009 Jun 16.

Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, 9 Quai Moncousu, 44093 Nantes Cedex 1, France.

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http://dx.doi.org/10.1210/jc.2009-0226DOI Listing
September 2009

[Monozygotic heterocaryotic twins: prenatal diagnosis and management].

Presse Med 2009 Jul-Aug;38(7-8):1170-3. Epub 2009 Apr 17.

Pôle Mère-Enfant (Obstétrique et Pédiatrie) et Service de Génétique, CHU Nantes, F-44093 Nantes, France.

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http://dx.doi.org/10.1016/j.lpm.2008.12.032DOI Listing
July 2009

Complex constitutional subtelomeric 1p36.3 deletion/duplication in a mentally retarded child with neonatal neuroblastoma.

Eur J Med Genet 2008 Nov-Dec;51(6):679-84. Epub 2008 Jul 11.

Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes Cedex 1, France.

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http://dx.doi.org/10.1016/j.ejmg.2008.06.004DOI Listing
March 2009

A 8.26Mb deletion in 6q16 and a 4.95Mb deletion in 20p12 including JAG1 and BMP2 in a patient with Alagille syndrome and Wolff-Parkinson-White syndrome.

Eur J Med Genet 2008 Nov-Dec;51(6):651-7. Epub 2008 Aug 15.

CHU de Nantes, Service de Cardiologie, Nantes, France; INSERM, UMR915, l'institut du thorax, Nantes, France; CNRS, ERL3147, Nantes, France; Université de Nantes, Nantes, France.

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http://dx.doi.org/10.1016/j.ejmg.2008.07.012DOI Listing
March 2009