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There are 30312 results for: content related to: High-resolution I maging of the M/S D odekanisos S hipwreck S ite off D eveboynu B urnu, T urkey

  1. A novel mutation (g.106737G>T) in zone of polarizing activity regulatory sequence (ZRS) causes variable limb phenotypes in Werner mesomelia

    American Journal of Medical Genetics Part A

    Volume 164, Issue 4, April 2014, Pages: 898–906, Katta M. Girisha, Abdul Mueed Bidchol, Preeti S. Kamath, Krupa H. Shah, Geert R. Mortier, Stefan Mundlos and Hitesh Shah

    Article first published online : 29 JAN 2014, DOI: 10.1002/ajmg.a.36367

  2. Determination of salbutamol and salbutamol glucuronide in human urine by means of liquid chromatography-tandem mass spectrometry

    Drug Testing and Analysis

    Volume 3, Issue 11-12, November-December 2011, Pages: 820–827, Ute Mareck, Sven Guddat, Anne Schwenke, Simon Beuck, Hans Geyer, Ulrich Flenker, Jimmi Elers, Vibeke Backer, Mario Thevis and Wilhelm Schänzer

    Article first published online : 14 NOV 2011, DOI: 10.1002/dta.367

  3. Fullerenes: Metal Complexes

    Standard Article

    Encyclopedia of Inorganic Chemistry

    Alan L. Balch and Christopher J. Chancellor

    Published Online : 15 MAR 2009, DOI: 10.1002/0470862106.ia367

  4. Oligohydramnios sequence revisited in relationship to arthrogryposis, with distinctive skin changes

    American Journal of Medical Genetics Part A

    Volume 164, Issue 11, November 2014, Pages: 2775–2792, Judith G. Hall

    Article first published online : 26 AUG 2014, DOI: 10.1002/ajmg.a.36731

  5. The Roman Shipwreck of Antirhodos Island in the Portus Magnus of Alexandria, Egypt

    International Journal of Nautical Archaeology

    Volume 42, Issue 1, March 2013, Pages: 44–59, Patrice Sandrin, Alexander Belov and David Fabre

    Article first published online : 16 OCT 2012, DOI: 10.1111/j.1095-9270.2012.00363.x

  6. Maritime Site Protection and the Fetch Method: an example from Rogaland, Norway

    International Journal of Nautical Archaeology

    Volume 42, Issue 1, March 2013, Pages: 87–102, Marianne Nitter, Endre Elvestad and Lotte Selsing

    Article first published online : 18 OCT 2012, DOI: 10.1111/j.1095-9270.2012.00365.x

  7. A Late-18th-Century Merchantman Wrecked in the South Edinburgh Channel, Thames Estuary, England

    International Journal of Nautical Archaeology

    Volume 42, Issue 1, March 2013, Pages: 137–149, David Parham, Elizabeth Rundell and Pieter van der Merwe

    Article first published online : 16 OCT 2012, DOI: 10.1111/j.1095-9270.2012.00364.x

  8. Subterranean Maritime Archaeology in Sigtuna, Sweden: excavated evidence of Viking Age boat building and repair

    International Journal of Nautical Archaeology

    Volume 42, Issue 1, March 2013, Pages: 196–204, Rune Edberg

    Article first published online : 4 FEB 2013, DOI: 10.1111/j.1095-9270.2012.00366.x

  9. You have free access to this content
    Immune mediated disorders in women with a fragile X expansion and FXTAS

    American Journal of Medical Genetics Part A

    Volume 167, Issue 1, January 2015, Pages: 190–197, Isha Jalnapurkar, Nuva Rafika, Flora Tassone and Randi Hagerman

    Article first published online : 14 NOV 2014, DOI: 10.1002/ajmg.a.36748

  10. Duodenal atresia in 17q12 microdeletion including HNF1B: A new associated malformation in this syndrome

    American Journal of Medical Genetics Part A

    Volume 164, Issue 12, December 2014, Pages: 3076–3082, Fabiola Quintero-Rivera, Jennifer S. Woo, Eric M. Bomberg, W. Dean Wallace, Jane Peredo and Katrina M. Dipple

    Article first published online : 24 SEP 2014, DOI: 10.1002/ajmg.a.36767

  11. NDST1 missense mutations in autosomal recessive intellectual disability

    American Journal of Medical Genetics Part A

    Volume 164, Issue 11, November 2014, Pages: 2753–2763, Miriam S. Reuter, Luciana Musante, Hao Hu, Stefan Diederich, Heinrich Sticht, Arif B. Ekici, Steffen Uebe, Thomas F. Wienker, Oliver Bartsch, Ulrich Zechner, Cornelia Oppitz, Krystyna Keleman, Rami Abou Jamra, Hossein Najmabadi, Susann Schweiger, André Reis and Kimia Kahrizi

    Article first published online : 14 AUG 2014, DOI: 10.1002/ajmg.a.36723

  12. ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelination

    American Journal of Medical Genetics Part A

    Volume 164, Issue 11, November 2014, Pages: 2892–2900, Laila Shehata, Dimitre R. Simeonov, Anja Raams, Lynne Wolfe, Adeline Vanderver, Xueli Li, Yan Huang, Shannon Garner, Cornelius F. Boerkoel, Audrey Thurm, Gail E. Herman, Cynthia J. Tifft, Miao He, Nicolaas G.J. Jaspers and William A. Gahl

    Article first published online : 22 SEP 2014, DOI: 10.1002/ajmg.a.36709

  13. Identification of TBX5 mutations in a series of 94 patients with Tetralogy of Fallot

    American Journal of Medical Genetics Part A

    Volume 164, Issue 12, December 2014, Pages: 3100–3107, Anwar Baban, Alex Vincent Postma, Monica Marini, Gianluca Trocchio, Antonella Santilli, Monica Pelegrini, Pietro Sirleto, Margherita Lerone, Sonia Bernadette Albanese, Phil Barnett, Cornelis Job Boogerd, Bruno Dallapiccola, Maria Cristina Digilio, Roberto Ravazzolo and Giacomo Pongiglione

    Article first published online : 26 SEP 2014, DOI: 10.1002/ajmg.a.36783

  14. Neural tube defects and atypical deletion on 22q11.2

    American Journal of Medical Genetics Part A

    Volume 164, Issue 11, November 2014, Pages: 2701–2706, Chiara Leoni, David A. Stevenson, Katherine B. Geiersbach, Christian N. Paxton, Bryan L. Krock, Rong Mao and Alan F. Rope

    Article first published online : 13 AUG 2014, DOI: 10.1002/ajmg.a.36701

  15. Unusually severe hypophosphatemic rickets caused by a novel and complex re-arrangement of the PHEX gene

    American Journal of Medical Genetics Part A

    Volume 164, Issue 11, November 2014, Pages: 2931–2937, Tuula Pekkarinen, Bettina Lorenz-Depiereux, Martina Lohman and Outi Mäkitie

    Article first published online : 13 AUG 2014, DOI: 10.1002/ajmg.a.36721

  16. Oculoectodermal syndrome: Report of a new case with a broad clinical spectrum

    American Journal of Medical Genetics Part A

    Volume 164, Issue 11, November 2014, Pages: 2947–2951, Deniz Aslan, Rustu Fikret Akata, Julia Schröder, Rudolf Happle, Ute Moog and Oliver Bartsch

    Article first published online : 22 SEP 2014, DOI: 10.1002/ajmg.a.36727

  17. Cognitive-motor profile, clinical characteristics and diagnosis of CHARGE syndrome: An Italian experience

    American Journal of Medical Genetics Part A

    Volume 164, Issue 12, December 2014, Pages: 3042–3051, Lucia Santoro, Anna Ficcadenti, Federica Zallocco, Giada Del Baldo, Francesca Piraccini, Rosaria Gesuita, Patrizia Ceccarani and Orazio Gabrielli

    Article first published online : 24 SEP 2014, DOI: 10.1002/ajmg.a.36758

  18. You have free access to this content
    Genotype-phenotype relationships in Freeman–Sheldon syndrome

    American Journal of Medical Genetics Part A

    Volume 164, Issue 11, November 2014, Pages: 2808–2813, Anita E. Beck, Margaret J. McMillin, Heidi I. S. Gildersleeve, Kathryn M. B. Shively, Andy Tang and Michael J. Bamshad

    Article first published online : 25 SEP 2014, DOI: 10.1002/ajmg.a.36762

  19. Distal arthrogryposis type 5D with a novel ECEL1 gene mutation

    American Journal of Medical Genetics Part A

    Volume 164, Issue 11, November 2014, Pages: 2857–2862, Siddaramappa J. Patil, Gaurava Kumar Rai, Venkatraman Bhat, Vakkalagadda A. Ramesh, H.A. Nagarajaram, Jyoti Matalia and Shubha R. Phadke

    Article first published online : 5 AUG 2014, DOI: 10.1002/ajmg.a.36702