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101

Cytogenetic investigation of a child with a mosaic isochromosome 18q and ring 18q

Noëlle Souraty, Damien Sanlaville, Rima Chédid, Marc Le Lorc'h, Marie-Laure Maurin, Lola Ghanem, Sabine Maalouf, Michel Vekemans, André Mégarbané

Journal:

European Journal of Medical Genetics

Year:

2007

Language:

english

File:

PDF, 667 KB

english, 2007

102

Pure proximal deletion of chromosome 21 and kyphosis

Boris Keren, Céline Bernardin, Annick Toutain, Delphine Heron, Bernard Fouquet, Béatrice Laudier, Louise Telvi, Serge Pierrick Romana, Michel Vekemans, Damien Sanlaville

Journal:

European Journal of Medical Genetics

Year:

2007

Language:

english

File:

PDF, 138 KB

english, 2007

103

Program/Abstract # 500

Christelle Golzio, Emmanuelle Havis, Gregory Nuel, Candice Babarit, Arnold Munnich, Michel Vekemans, Stanislas Lyonnet, Heather Etchevers

Journal:

Developmental Biology

Year:

2009

Language:

english

File:

PDF, 51 KB

english, 2009

104

Should PMM2-deficiency (CDG Ia) be searched in every case of unexplained hydrops fetalis?

Nadia Léticée, Bettina Bessières-Grattagliano, Thierry Dupré, Sandrine Vuillaumier-Barrot, Pascale de Lonlay, Ferechté Razavi, Nadia El Khartoufi, Yves Ville, Michel Vekemans, Raymonde Bouvier, Nathal

Journal:

Molecular Genetics and Metabolism

Year:

2010

Language:

english

File:

PDF, 519 KB

english, 2010

105

Postoperative radiotherapy after radical prostatectomy: a randomised controlled trial (EORTC trial 22911)

Michel Bolla, Hein van Poppel, Laurence Collette, Paul van Cangh, Kris Vekemans, Luigi Da Pozzo, Theo M de Reijke, Antony Verbaeys, Jean-François Bosset, Roland van Velthoven, Jean-Marie Maréchal, Pie

Journal:

Year:

2005

Language:

english

File:

PDF, 111 KB

english, 2005

106

Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome

Hélène De Leersnyder, Marie-Christine de Blois, Bruno Claustrat, Serge Romana, Urs Albrecht, Jürgen-Christoph von Kleist-Retzow, Bruno Delobel, Géraldine Viot, Stanislas Lyonnet, Michel Vekemans, Arno

Journal:

The Journal of Pediatrics

Year:

2001

Language:

english

File:

PDF, 109 KB

english, 2001

107

Recurrent Williams-Beuren Syndrome in a Sibship Suggestive of Maternal Germ-Line Mosaicism

Ali Kara-Mostefa, Odile Raoul, Stanislas Lyonnet, Jeanne Amiel, Arnold Munnich, Michel Vekemans, Suzel Magnier, Batool Ossareh, Jean-Paul Bonnefont

Journal:

The American Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 256 KB

english, 1999

108

Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy

Florence Molinari, Annick Raas-Rothschild, Marlène Rio, Giuseppe Fiermonte, Ferechté Encha-Razavi, Luigi Palmieri, Ferdinando Palmieri, Ziva Ben-Neriah, Noman Kadhom, Michel Vekemans, Tania Attié-Bita

Journal:

The American Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 6.16 MB

english, 2005

109

Genetics of Developmental Disabilities.

Michel Vekemans

Journal:

The American Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 38 KB

english, 2005

110

Helical self-assembly and co-assembly of fluorinated, preorganized discotics

van Houtem, Michel H. C. J., Benaskar, Faysal, Fitié, Carel F. C., Martín-Rapún, Rafael, Vekemans, Jef A. J. M., Meijer, E. W.

Journal:

Organic & Biomolecular Chemistry

Year:

2012

Language:

english

File:

PDF, 1.92 MB

english, 2012

111

Regional and cellular specificity of the expression of TPRD, the tetratricopeptide Down syndrome gene, during human embryonic development

Mohammed Rachidi, Carmela Lopes, Svetlana Gassanova, Pierre-Marie Sinet, Michel Vekemans, Tania Attie, Anne-Lise Delezoide, Jean-Maurice Delabar

Journal:

Mechanisms of Development

Year:

2000

Language:

english

File:

PDF, 2.52 MB

english, 2000

112

Expression of the SMADIP1 gene during early human development

Yolanda Espinosa-Parrilla, Jeanne Amiel, Joëlle Augé, Férechté Encha-Razavi, Arnold Munnich, Stanislas Lyonnet, Michel Vekemans, Tania Attié-Bitach

Journal:

Mechanisms of Development

Year:

2002

Language:

english

File:

PDF, 459 KB

english, 2002

113

Editorial

Vekemans, Michel

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2013

Language:

english

File:

PDF, 39 KB

english, 2013

114

splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3

Douglas J. Epstein, Michel Vekemans, Philippe Gros

Journal:

Year:

1991

Language:

english

File:

PDF, 2.59 MB

english, 1991

115

Genetic models of carcinogenesis

Robert P. Bolande, Michel J.-J. Vekemans

Journal:

Human Pathology

Year:

1983

Language:

english

File:

PDF, 484 KB

english, 1983

116

Long-Term Follow-Up of the Imatinib GRAAPH-2003 Study in Newly Diagnosed Patients with De Novo Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia: A GRAALL Study

Tanguy-Schmidt, Aline, Rousselot, Philippe, Chalandon, Yves, Cayuela, Jean-Michel, Hayette, Sandrine, Vekemans, Marie-Christiane, Escoffre, Martine, Huguet, Françoise, Réa, Delphine, Delannoy, André,

Journal:

Biology of Blood and Marrow Transplantation

Year:

2013

Language:

english

File:

PDF, 605 KB

english, 2013

117

Molecular characterization of a deletion encompassing the splotch mutation on mouse chromosome 1

Epstein, Douglas J., Malo, Danielle, Vekemans, Michel, Gros, Philippe

Journal:

Year:

1991

Language:

english

File:

PDF, 946 KB

english, 1991

118

Chorionic villi sampling: Clinical experience, immediate complications, and patient attitudes

Perry, Tracy B., Vekemans, Michel J.J., Lippman, Abby, Hamilton, Emily F., Fournier, Paul J.R.

Journal:

American Journal of Obstetrics and Gynecology

Year:

1985

Language:

english

File:

PDF, 600 KB

english, 1985

119

The host resistance locus Bcg is tightly linked to a group of cytoskeleton-associated protein genes that include villin and desmin

Malo, Danielle, Schurr, Erwin, Epstein, Douglas J., Vekemans, Michel, Skamene, Emil, Gros, Philippe

Journal:

Year:

1991

Language:

english

File:

PDF, 954 KB

english, 1991

120

Identification and mapping of six microdissected genomic DNA probes to the proximal region of mouse chromosome 1

Vidal, Silvia M., Epstein, Douglas J., Malo, Danielle, Weith, Andreas, Vekemans, Michel, Gros, Philippe

Journal:

Year:

1992

Language:

english

File:

PDF, 1.05 MB

english, 1992

121

Synthesis of 3,6-Diaminophthalimides for Ureidophthalimide-Based Foldamers

Sinkeldam, Renatus W., van Houtem, Michel H. C. J., Koeckelberghs, Guy, Vekemans, Jef A. J. M., Meijer, E. W.

Journal:

Organic Letters

Year:

2006

Language:

english

File:

PDF, 70 KB

english, 2006

122

An infant with Down syndrome and retinoblastoma A possible non-fortuitous association

Satgé, Daniel, Gembara, Piotr, Sasco, Annie J., Francannet, Christine, Desjardins, Laurence, Vekemans, Michel, Demeocq, François

Journal:

Ophthalmic Genetics

Year:

2001

Language:

english

File:

PDF, 115 KB

english, 2001

123

Book review

Vekemans, Michel

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2013

Language:

english

File:

PDF, 38 KB

english, 2013

124

Contiguous gene deletion of TBX5 and TBX3 leads to a varible phenotype with combined features of holt-oram and ulnar-mammary syndromes

Alby, Caroline, Bessieres, Bettina, Bieth, Eric, Attie-Bitach, Tania, Fermont, Laurent, Citony, Isabelle, Razavi, Ferechté, Vekemans, Michel, Escande, Fabienne, Manouvrier, Sylvie, Malan, Valérie, Ami

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 1.72 MB

english, 2013

125

Use of in Situ Hybridization in Clinical Cytogenetics

Zahed, Laila, Vekemans, Michel

Journal:

Fetal and Pediatric Pathology

Year:

1991

Language:

english

File:

PDF, 620 KB

english, 1991

126

Chromosome banding studies of the osprey Pandion haliaetus (Aves, Falconiformes)

Kohler, C. Deborah, Schaadt, Charles P., Vekemans, Michel J. J.

Journal:

Year:

1989

Language:

english

File:

PDF, 316 KB

english, 1989

127

Identification of the IRXB Gene Cluster as Candidate Genes in Severe Dysgenesis of the Ocular Anterior Segment

Chaabouni, Myriam, Etchevers, Heather, De Blois, Marie Christine, Calvas, Patrick, Waill-Perrier, Marie Christine, Vekemans, Michel, Romana, Serge Pierrick

Journal:

Investigative Ophthalmology & Visual Science

Year:

2010

Language:

english

File:

PDF, 1.27 MB

english, 2010

128

Economic burden of brain metastases among patients with metastatic melanoma in a USA managed care population

Vekeman, Francis, Cloutier, Michel, Yermakov, Sander, Amonkar, Mayur M., Arondekar, Bhakti, Duh, Mei S.

Journal:

Melanoma Research

Year:

2014

Language:

english

File:

PDF, 484 KB

english, 2014

129

HLA‐B*35–Restricted CD8 T Cell Epitopes in the Antigen 85 Complex of Mycobacterium tuberculosis

Klein, Michèl R., Smith, Steven M., Hammond, Abdulrahman S., Ogg, Graham S., King, Abigail S., Vekemans, Johan, Jaye, Assan, Lukey, Pauline T., McAdam, Keith P. W. J.

Journal:

The Journal of Infectious Diseases

Year:

2001

Language:

english

File:

PDF, 152 KB

english, 2001

130

PAX8 , TITF1 , and FOXE1 Gene Expression Patterns during Human Development: New Insights into Human Thyroid Development and Thyroid Dysgenesis-Associated Malformations

Trueba, Sylvia Sura, Augé, Joëlle, Mattei, Géraldine, Etchevers, Heather, Martinovic, Jélééna, Czernichow, Paul, Vekemans, Michel, Polak, Michel, Attié-Bitach, Tania

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2005

Language:

english

File:

PDF, 809 KB

english, 2005

131

A survey of ocular tumors in Down syndrome alone or associated with another genetic affection

Satgé, Daniel, Lacombe, Didier, Vekemans, Michel JJ, Bonnet, Anne, Réthoré, Marie-Odile, Munier, Francis

Journal:

International Journal on Disability and Human Development

Year:

2006

Language:

english

File:

PDF, 1.03 MB

english, 2006

132

A review of malignancies in fragile X syndrome and report of an Ewing sarcoma

Satgé, Daniel, Vérité, Cécile, Bui, Binh Nguyen, Perel, Yves, Taine, Laurence, Vekemans, Michel, Lacombe, Didier

Journal:

International Journal on Disability and Human Development

Year:

2008

Language:

english

File:

PDF, 644 KB

english, 2008

133

17q21.31 Microdeletion: Brain Anomalies Leading to Prenatal Diagnosis

Egloff, Matthieu, Encha-Razavi, Ferechte, Garel, Catherine, Bonni�re-Darcy, Maryse, Millischer, Anne-Elodie, Lapierre, Jean-Michel, Fontaine, Sophie, de Blois, Marie-Christine, Vekemans, Michel, Turle

Journal:

Cytogenetic and Genome Research

Year:

2014

Language:

english

File:

PDF, 139 KB

english, 2014

134

Book Review Genetic Disorders and the Fetus: Diagnosis, Prevention, and Treatment Fifth edition. Edited by Aubrey Milunsky. 1224 pp., illustrated. Baltimore, Johns Hopkins University Press, 2004. $225. 0-8018-7928-0

Vekemans, Michel

Journal:

Boston Medical and Surgical Journal

Year:

2005

Language:

english

File:

PDF, 57 KB

english, 2005

135

Is Blood Testing Necessary before OC Prescription in Africa?

Pierre Buekens, Marcel Vekemans, Bruno Dujardin, Michel Boutsen and Elizabeth Wollast

Journal:

Studies in Family Planning

Year:

1990

Language:

english

File:

PDF, 492 KB

english, 1990

136

Specific 1,25-Hydroxycholecalciferol Receptors and Stimulation of 25-Hydroxycholecalciferol- 24R Hydroxylase in Human Amniotic Cells

Delvin, Edgard E, Pilon, Anne-Marie, Vekemans, Michel

Journal:

Pediatric Research

Year:

1987

Language:

english

File:

PDF, 453 KB

english, 1987

137

Cytogenetics: Basic and Applied Aspectsby Günter Obe; Armin Basler

Review by: Michel Vekemans

Journal:

American Scientist

Year:

1990

Language:

english

File:

PDF, 350 KB

english, 1990

138

Long-Chain Fatty Acid Oxidation during Early Human Development

Oey, Nadia A, den boer, Margarethe E J, Wijburg, Frits A, Vekemans, Michel, Augé, Jołle, Steiner, Céline, Wanders, Ronald J A, Waterham, Hans R, Ruiter, Jos P N, Attié-Bitach, Tania

Journal:

Pediatric Research

Year:

2005

Language:

english

File:

PDF, 1.17 MB

english, 2005

139

Fetal Intestinal Obstruction Induces Alteration of Enteric Nervous System Development in Human Intestinal Atresia

Khen, Naziha, Jaubert, Francis, Sauvat, Frederique, Fourcade, Laurent, Jan, Dominique, Martinovic, Jelena, Vekemans, Michel, Landais, Paul, Brousse, Nicole, Leborgne, Michele, Nihoul-Fékété, Claire, C

Journal:

Pediatric Research

Year:

2004

Language:

english

File:

PDF, 1.79 MB

english, 2004

140

A Fetus with Down Syndrome and Intratubular Germ Cell Neoplasia

Satgé, Daniel, Jacobsen, Grete Krag, Cessot, Françoise, Raffi, Fernand, Vekemans, Michel

Journal:

Fetal and Pediatric Pathology

Year:

1996

File:

PDF, 1.02 MB

1996

141

A Fetus with Down Syndrome and Intratubular Germ Cell Neoplasia

Satgé, Daniel, Jacobsen, Grete Krag, Cessot, Françoise, Raffi, Fernand, Vekemans, Michel

Journal:

Fetal and Pediatric Pathology

Year:

1996

Language:

english

File:

PDF, 1.02 MB

english, 1996

142

Reviewers list

Vekemans, Michel

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2015

Language:

english

File:

PDF, 41 KB

english, 2015

143

Growth rate of follicular estrogen secretion in relation to the outcome of in vitro fertilization and embryo replacement

Dirnfeld, Martha, Lejeune, Bernard, Camus, Michel, Vekemans, Marcel, Leroy, Fernand

Journal:

Fertility and Sterility

Year:

1985

Language:

english

File:

PDF, 731 KB

english, 1985

144

La duplication Xq25 : rôle crucial du gène STAG2 dans cette nouvelle cohésinopathie

Leroy, Camille, Jacquemont, Marie-Line, Doray, Bérénice, Lamblin, Denis, Cormier Daire, Valérie, Philippe, Anne, Patrat, Catherine, Steffan, Julie, Colleaux, Laurence, Vekemans, Michel, Romana, Serge,

Journal:

Year:

2015

Language:

french

File:

PDF, 59 KB

french, 2015

145

In vitro fertilization and embryo transfer as related to endogenous luteinizing hormone rise or human chorionic gonadotropin administration**Supported by the Fonds National de la Recherche Scientifique and the Fonds de la Recherche Scientifique Médicale (Belgium).

Lejeune, Bernard, Degueldre, Michel, Camus, Michel, Vekemans, Marcel, Opsomer, Luc, Leroy, Fernand

Journal:

Fertility and Sterility

Year:

1986

Language:

english

File:

PDF, 1.02 MB

english, 1986

146

The rat phospholipase Cβ 4 gene is expressed at high abundance in cerebellar Purkinje cells

Roustan, Paul, Abitbol, Marc, Ménini, Christian, Ribeaudeau, Florence, Gérard, Marion, Vekemans, Michel, Mallet, Jacques, Dufier, Jean-Louis

Journal:

Year:

1995

File:

PDF, 410 KB

1995

147

First fetal case of the 8q24.3 contiguous genes syndrome

Wells, Constance, Spaggiari, Emmanuel, Malan, Valérie, Stirnemann, Julien J., Attie-Bitach, Tania, Ville, Yves, Vekemans, Michel, Bessieres, Bettina, Romana, Serge

Journal:

American Journal of Medical Genetics Part A

Year:

2016

Language:

english

File:

PDF, 1.43 MB

english, 2016

148

A tumor profile in Edwards syndrome (trisomy 18)

Satgé, Daniel, Nishi, Motoi, Sirvent, Nicolas, Vekemans, Michel

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Year:

2016

Language:

english

File:

PDF, 132 KB

english, 2016

149

Higher pregnancy rates after in vitro fertilization and embryo transfer in cases with sperm defects

Englert, Yvon, Vekemans, Marcel, Lejeune, Bernard, Rysselberge, Michel Van, Puissant, Françoise, Degueldre, Michel, Leroy, Fernand

Journal:

Fertility and Sterility

Year:

1987

Language:

english

File:

PDF, 491 KB

english, 1987

150

A unified birth defects research

Daston, George P., Tuan, Rocky S., Vekemans, Michel

Journal:

Birth Defects Research

Year:

2017

Language:

english

File:

PDF, 33 KB

english, 2017