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There are 8127278 results for: content related to: Maternal Encounters: The Ethics of Interruption. By LISA BARAITSER and Feminist Mothering in Theory and Practice, 1985–1995: A Study in Transformative Politics. By FIONA JOY GREEN and Feminist Art and the Maternal. By ANDREA LISS

  1. You have free access to this content
    Nicolaides–Baraitser syndrome: Delineation of the phenotype

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 8, August 2009, Pages: 1628–1640, Sérgio B. Sousa, Omar A. Abdul-Rahman, Armand Bottani, Valérie 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 and Raoul C.M. Hennekam

    Version of Record online : 15 JUL 2009, DOI: 10.1002/ajmg.a.32956

  2. Temple–Baraitser syndrome: A rare and possibly unrecognized condition

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 9, September 2010, Pages: 2322–2326, Adeline Jacquinet, Marion Gérard, Michael T. Gabbett, Léon Rausin, Jean-Paul Misson, Björn Menten, Geert Mortier, Lionel Van Maldergem, Alain Verloes and François-Guillaume Debray

    Version of Record online : 3 AUG 2010, DOI: 10.1002/ajmg.a.33574

  3. OFD II, OFD VI, and Joubert syndrome manifestations in 2 sibs

    American Journal of Medical Genetics

    Volume 91, Issue 2, 13 March 2000, Pages: 135–137, Karsten Haug, Saima Khan, Sigrun Fuchs and Rainer König

    Version of Record online : 4 APR 2000, DOI: 10.1002/(SICI)1096-8628(20000313)91:2<135::AID-AJMG11>3.0.CO;2-1

  4. Acute myeloid leukemia in Baraitser–Winter cerebrofrontofacial syndrome

    American Journal of Medical Genetics Part A

    Volume 173, Issue 2, February 2017, Pages: 546–549, Paola Cianci, Grazia Fazio, Sara Casagranda, Marco Spinelli, Carmelo Rizzari, Gianni Cazzaniga and Angelo Selicorni

    Version of Record online : 21 NOV 2016, DOI: 10.1002/ajmg.a.38057

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    Color atlas of congenital malformation syndromes By M. Baraitser and R. M. Winter Published by Mosby-Wolfe, 1996, 246 pp. ISBN 0-72342-0734

    Ultrasound in Obstetrics & Gynecology

    Volume 7, Issue 5, May 1996, Page: 388, B. Benacerraf

    Version of Record online : 18 FEB 2003, DOI: 10.1046/j.1469-0705.1996.07050388.x

  6. Baraitser–Winter cerebrofrontofacial syndrome

    Clinical Genetics

    T.M. Yates, C.L. Turner, H.V. Firth, J. Berg and D.T. Pilz

    Version of Record online : 30 NOV 2016, DOI: 10.1111/cge.12864

  7. Nonspecific X-linked mental retardation with macrocephaly and obesity: A further family

    American Journal of Medical Genetics

    Volume 57, Issue 3, 3 July 1995, Pages: 380–384, M. Baraitser, Dr. W. Reardon and S. Vijeratnam

    Version of Record online : 9 JUN 2005, DOI: 10.1002/ajmg.1320570303

  8. The genetics of neurological disorders (oxford monographs on medical genetics) By M. Baraitser New York, oxford university press, 1982 528 pp, ilhstrated, $69.00

    Annals of Neurology

    Volume 15, Issue 4, April 1984, Page: 407, Fred Plum

    Version of Record online : 7 OCT 2004, DOI: 10.1002/ana.410150424

  9. Clinical and molecular features of Joubert syndrome and related disorders

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

    Volume 151C, Issue 4, 15 November 2009, Pages: 326–340, Melissa A. Parisi

    Version of Record online : 28 OCT 2009, DOI: 10.1002/ajmg.c.30229

  10. Regarding the ongoing discussion about the reporting of single cases

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 12, 15 June 2007, Page: 1262, Michael Baraitser

    Version of Record online : 15 MAY 2007, DOI: 10.1002/ajmg.a.31708

  11. Moebius sequence and hypogonadotrophic hypogonadism

    American Journal of Medical Genetics Part A

    Volume 123A, Issue 1, November 15, 2003, Pages: 107–110, Juliet E. Jennings, Colm Costigan and William Reardon

    Version of Record online : 18 SEP 2003, DOI: 10.1002/ajmg.a.20500

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    Update on the ACTG1-associated Baraitser–Winter cerebrofrontofacial syndrome

    American Journal of Medical Genetics Part A

    Volume 170, Issue 10, October 2016, Pages: 2644–2651, Nataliya Di Donato, Alma Kuechler, Samantha Vergano, Wolfram Heinritz, Joann Bodurtha, Sabiha R. Merchant, Galen Breningstall, Roger Ladda, Susan Sell, Janine Altmüller, Nina Bögershausen, Andrew E. Timms, Karl Hackmann, Evelin Schrock, Sarah Collins, Carissa Olds, Andreas Rump and William B. Dobyns

    Version of Record online : 30 MAY 2016, DOI: 10.1002/ajmg.a.37771

  13. On Saraiva and Baraitser and Joubert syndrome: A review

    American Journal of Medical Genetics

    Volume 46, Issue 6, 1 July 1993, Page: 732, Dr. M. di Rocco

    Version of Record online : 3 JUN 2005, DOI: 10.1002/ajmg.1320460630

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    Lumping of CFC and Baraitser-Patton Noonan-Like syndromes

    American Journal of Medical Genetics

    Volume 42, Issue 5, 1 March 1992, Page: 756, Dr. Alain Verloes and Martine Le Merrer

    Version of Record online : 7 JUN 2005, DOI: 10.1002/ajmg.1320420529

  15. Response to Olney et al.—“Limb/Pelvis hypoplasia/aplasia with skull defect (Schinzel phocomelia): Distinctive features and prenatal detection”

    American Journal of Medical Genetics

    Volume 111, Issue 4, 1 September 2002, Page: 457, Robin Winter

    Version of Record online : 15 JUL 2002, DOI: 10.1002/ajmg.10502

  16. Costello syndrome: Report and review

    American Journal of Medical Genetics

    Volume 82, Issue 2, 15 January 1999, Pages: 187–193, Agnies M. van Eeghen, Ietje van Gelderen and Raoul C.M. Hennekam

    Version of Record online : 29 JAN 1999, DOI: 10.1002/(SICI)1096-8628(19990115)82:2<187::AID-AJMG17>3.0.CO;2-2

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    Dystonia-deafness syndrome caused by a β-actin gene mutation and response to deep brain stimulation

    Movement Disorders

    Volume 32, Issue 1, January 2017, Pages: 162–165, Hendriekje Eggink, Martje E. van Egmond, Corien C. Verschuuren-Bemelmans, Marleen C. Schönherr, Tom J. de Koning, D.L. Marinus Oterdoom, J. Marc C. van Dijk and Marina A.J. Tijssen

    Version of Record online : 8 NOV 2016, DOI: 10.1002/mds.26842

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    New SMARCA2 mutation in a patient with Nicolaides–Baraitser syndrome and myoclonic astatic epilepsy

    American Journal of Medical Genetics Part A

    Volume 173, Issue 1, January 2017, Pages: 195–199, S. Tang, E. Hughes, K. Lascelles, EuroEPINOMICS RES myoclonic astatic epilepsy working group, M. A. Simpson and D. K. Pal

    Version of Record online : 26 SEP 2016, DOI: 10.1002/ajmg.a.37935

  19. The genetics of neurological disorders Michael Baraitser. Oxford Monographics on Medical Genetics. Oxford University Press, New York, Toronto, 1982. $69.00

    American Journal of Medical Genetics

    Volume 16, Issue 3, November 1983, Pages: 448–449, Peggy A. Hanson

    Version of Record online : 2 JUN 2005, DOI: 10.1002/ajmg.1320160315

  20. Deafness associated with bilateral facial diplegia, ptosis and hypermobile joints—A new autosomal recessive condition?

    American Journal of Medical Genetics Part A

    Volume 122A, Issue 1, 15 September 2003, Pages: 84–88, William Reardon, Mairead McGinn, Mary D. King and Michael Earley

    Version of Record online : 6 MAY 2003, DOI: 10.1002/ajmg.a.20278