41
TITLE: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice  Full Text
AUTHORS: Joe Rainger; Ellen van Beusekom; Jacqueline K Ramsay; Lisa McKie; Lihadh Al Gazali; Rosanna Pallotta; Anita Saponari; Peter Branney; Malcolm Fisher; Harris Morrison; Louise Bicknell; Philippe Gautier; Paul Perry; Kishan Sokhi; David Sexton; Tanya M Bardakjian; Adele S Schneider; Nursel Elcioglu; Ferda Ozkinay; Rainer Koenig; Andre Megarbane; Nur N Semerci; Ayesha Khan; Saemah Zafar; Raoul Hennekam; Sergio B Sousa; Lina Ramos; Livia Garavelli; Andrea Superti Furga; Anita Wischmeijer; Ian J Jackson; Gabriele Gillessen Kaesbach; Han G Brunner; Dagmar Wieczorek; Hans van Bokhoven; David R FitzPatrick; ...More
PUBLISHED: 2011, SOURCE: PLOS GENETICS, VOLUME: 7, ISSUE: 7
INDEXED IN: Scopus WOS CrossRef: 49
42
TITLE: Expanding the Skeletal Phenotype of Loeys-Dietz Syndrome  Full Text
AUTHORS: Sergio B Sousa; Karen Lambot Juhan; Marlene Rio; Genevieve Baujat; Vicken Topouchian; Nadine Hanna; Martine Le Merrer; Francis Brunelle; Arnold Munnich; Catherine Boileau; Valerie Cormier Daire;
PUBLISHED: 2011, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 155A, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 10
43
TITLE: Postnatal Growth Retardation, Facial Dysmorphism, Spondylocarpal Synostosis, Cardiac Defect, and Inner Ear Malformation (Cardiospondylocarpofacial Syndrome?)-A Distinct Syndrome?  Full Text
AUTHORS: Sergio B Sousa; Genevieve Baujat; Veronique Abadie; Damien Bonnet; Daniel Sidi; Arnold Munnich; Deborah Krakow; Valerie Cormier Daire;
PUBLISHED: 2010, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 152A, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 3
44
TITLE: Nicolaides-Baraitser Syndrome: Delineation of the Phenotype  Full Text
AUTHORS: Sergio B Sousa; Omar A Abdul Rahman; Armand Bottani; Valerie Cormier Daire; Alan Fryer; Gabriele Gillessen Kaesbach; Denise Horn; Dragana Josifova; Alma Kuechler; Melissa Lees; Kay MacDermot; Alex Magee; Fanny Morice Picard; Elizabeth Rosser; Ajoy Sarkar; Nora Shannon; Irene Stolte Dijkstra; Alain Verloes; Emma Wakeling; Louise Wilson; Raoul C M Hennekam; ...More
PUBLISHED: 2009, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 149A, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 33
45
TITLE: Further Delineation of Spondylometaphyseal Dysplasia With Cone-Rod Dystrophy  Full Text
AUTHORS: Sergio B Sousa; Isabelle Russell Eggitt; Christine Hall; Bryan D Hall; Raoul C M Hennekam;
PUBLISHED: 2008, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 146A, ISSUE: 24
INDEXED IN: Scopus WOS CrossRef: 8
46
TITLE: Pitt-Hopkins syndrome - clinical report
AUTHORS: Sergio Sousa; Cabral, A; Zweier, C; Venancio, M; Rauch, A; Saraiva, J;
PUBLISHED: 2007, SOURCE: British Human Genetics Conference in JOURNAL OF MEDICAL GENETICS, VOLUME: 44
INDEXED IN: WOS
47
TITLE: Haploinsufficiency of TCF4 causes syndromal mental retardation with intermittent hyperventilation (Pitt-Hopkins syndrome)
AUTHORS: Christiane Zweier; Maarit M Peippo; Juliane Hoyer; Sergio Sousa; Armand Bottani; Jill Clayton Smith; William Reardon; Jorge Saraiva; Alexandra Cabral; Ina Goehring; Koen Devriendt; Thomy de Ravel; Emilia K Bijlsma; Raoul C M Hennekam; Alfredo Orrico; Monika Cohen; Alexander Dreweke; Andre Reis; Peter Nuernberg; Anita Rauch;
PUBLISHED: 2007, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 80, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 146
48
TITLE: Infrared study of the acidic and basic forms of betaxolol  Full Text
AUTHORS: Joao Canotilho; Esteves de Castro, RA; Helena, M; Teixeira, SF; Luisa L P Leitao; Simoes Redinha, JS;
PUBLISHED: 2006, SOURCE: SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, VOLUME: 64, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 6
49
TITLE: Introduction
AUTHORS: Teixeira, A; Tavares, AT ;
PUBLISHED: 2006, SOURCE: Multinationals, Clusters and Innovation: Does Public Policy Matter?
INDEXED IN: Scopus
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