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A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene

1994; Oxford University Press; Volume: 3; Issue: 10 Linguagem: Inglês

10.1093/hmg/3.10.1859

1460-2083

C. Vincent, Vasiliki Kalatzis, Sylvie Compain, Jacqueline Levilliers, Rima Slim, Fatima Graïa, Maria Lurdes Pereira, A Nivelon, Marie-France Croquette, Didier Lacombe, Jacqueline Vigneron, J Hélias, M. Broyer, David F. Callen, Eric Haan, Jean Weissenbach, Bruno Lacroix, Christine Bellané‐Chantelot, Denis Le Paslier, Daniel Cohen, Christine Petit,

Ophthalmology and Eye Disorders

Journal Article A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene Get access Christophe Vincent, Christophe Vincent Unité de Génétique Moléculaire Humaine (CNRS URA 1445), Institut Pasteur25 rue du Dr Roux, 75724 Paris Cédex 15 Search for other works by this author on: Oxford Academic PubMed Google Scholar Vasiliki Kalatzis, Vasiliki Kalatzis Unité de Génétique Moléculaire Humaine (CNRS URA 1445), Institut Pasteur25 rue du Dr Roux, 75724 Paris Cédex 15 Search for other works by this author on: Oxford Academic PubMed Google Scholar Sylvie Compain, Sylvie Compain Unité de Génétique Moléculaire Humaine (CNRS URA 1445), Institut Pasteur25 rue du Dr Roux, 75724 Paris Cédex 15 Search for other works by this author on: Oxford Academic PubMed Google Scholar Jacqueline Levilliers, Jacqueline Levilliers Unité de Génétique Moléculaire Humaine (CNRS URA 1445), Institut Pasteur25 rue du Dr Roux, 75724 Paris Cédex 15 Search for other works by this author on: Oxford Academic PubMed Google Scholar Rima Slim, Rima Slim Unité de Génétique Moléculaire Humaine (CNRS URA 1445), Institut Pasteur25 rue du Dr Roux, 75724 Paris Cédex 15 Search for other works by this author on: Oxford Academic PubMed Google Scholar Fatima Graia, Fatima Graia Unité de Génétique Moléculaire Humaine (CNRS URA 1445), Institut Pasteur25 rue du Dr Roux, 75724 Paris Cédex 15 Search for other works by this author on: Oxford Academic PubMed Google Scholar Maria de Lurdes Pereira, Maria de Lurdes Pereira Unité de Génétique Moléculaire Humaine (CNRS URA 1445), Institut Pasteur25 rue du Dr Roux, 75724 Paris Cédex 15 Search for other works by this author on: Oxford Academic PubMed Google Scholar Annie Nivelon, Annie Nivelon 1Centre de Génétique, Hopital d'Enfants10 Boulevard Maréchal-de-Lattre-de-Tassigny, 21034 Dijon Cédex Search for other works by this author on: Oxford Academic PubMed Google Scholar Marie-France Croquette, Marie-France Croquette 2Laboratoire de Cytogénétique, Hopital Saint Antoine329 Boulevard Victor Hugo, 59019 Lille Cédex Search for other works by this author on: Oxford Academic PubMed Google Scholar Didier Lacombe, Didier Lacombe 3Service de Pédiatrie et Génétique Médicale, Groupe Hospitalier Pellegrin-EnfantsPlace Amélie Raba-Léon, 33076 Bordeaux Cédex Search for other works by this author on: Oxford Academic PubMed Google Scholar ... Show more Jacqueline Vigneron, Jacqueline Vigneron 4Service de Néonatalogie-Génétique, Maternité Régionale de Nancy10 rue du Dr Heydenreich, 54042 Nancy Cédex Search for other works by this author on: Oxford Academic PubMed Google Scholar Jocelyne Helias, Jocelyne Helias 5Service d'Oto-Rhino-Laryngologie, Hopital Jean Minjoz25030 Besançon Cédex Search for other works by this author on: Oxford Academic PubMed Google Scholar Michel Broyer, Michel Broyer 6Département de Pédiatrie Médicale, Hopital Necker149 rue de Sérvres, 75743 Paris Cédex 15, France Search for other works by this author on: Oxford Academic PubMed Google Scholar David F. Callen, David F. Callen 7Department of Cytogenetics and Molecular Genetics, Adelaice Children's Hospital72 King William Road, North Adelaide, SA 5006, Australia Search for other works by this author on: Oxford Academic PubMed Google Scholar Eric A. Haan, Eric A. Haan 8Department of Medical Genetics, Adelaice Children's Hospital72 King William Road, North Adelaide, SA 5006, Australia Search for other works by this author on: Oxford Academic PubMed Google Scholar Jean Weissenbach, Jean Weissenbach 9Généthon, 1 rue de I'Internationale91000 Evry Search for other works by this author on: Oxford Academic PubMed Google Scholar Bruno Lacroix, Bruno Lacroix 10Centre d'Etude du Polymorphisme Humain27 rue Juliette Dodu, 75010 Paris, France Search for other works by this author on: Oxford Academic PubMed Google Scholar Christine Bellané-Chantelot, Christine Bellané-Chantelot 10Centre d'Etude du Polymorphisme Humain27 rue Juliette Dodu, 75010 Paris, France Search for other works by this author on: Oxford Academic PubMed Google Scholar Denis Le Paslier, Denis Le Paslier 10Centre d'Etude du Polymorphisme Humain27 rue Juliette Dodu, 75010 Paris, France Search for other works by this author on: Oxford Academic PubMed Google Scholar Daniel Cohen, Daniel Cohen 10Centre d'Etude du Polymorphisme Humain27 rue Juliette Dodu, 75010 Paris, France Search for other works by this author on: Oxford Academic PubMed Google Scholar Christine Petit Christine Petit * Unité de Génétique Moléculaire Humaine (CNRS URA 1445), Institut Pasteur25 rue du Dr Roux, 75724 Paris Cédex 15 *To whom correspondence should be addressed Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 3, Issue 10, October 1994, Pages 1859–1866, https://doi.org/10.1093/hmg/3.10.1859 Published: 01 October 1994 Article history Received: 22 June 1994 Revision received: 11 August 1994 Accepted: 11 August 1994 Published: 01 October 1994