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There are 9486 results for: content related to: Maritime Site Protection and the Fetch Method: an example from Rogaland, Norway

  1. 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

  2. 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

  3. 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

  4. Development of liquid chromatography-tandem mass spectrometry-based analytical assays for the determination of HIF stabilizers in preventive doping research

    Drug Testing and Analysis

    Volume 3, Issue 11-12, November-December 2011, Pages: 756–770, Simon Beuck, Wolfgang Bornatsch, Andreas Lagojda, Wilhelm Schänzer and Mario Thevis

    Article first published online : 29 DEC 2011, DOI: 10.1002/dta.365

  5. The Mollö Cog Re-Examined and Re-Evaluated

    International Journal of Nautical Archaeology

    Volume 41, Issue 2, September 2012, Pages: 372–389, Staffan von Arbin and Aoife Daly

    Article first published online : 30 MAR 2012, DOI: 10.1111/j.1095-9270.2012.00343.x

  6. Proposed regulations for research with biospecimens: Responses from stakeholders at CTSA consortium institutions

    American Journal of Medical Genetics Part A

    Volume 164, Issue 4, April 2014, Pages: 892–897, Jeffrey R. Botkin, Rebecca Anderson, Tom Murray, Laura M. Beskow, Karen Maschke and Leona Cuttler

    Article first published online : 23 JAN 2014, DOI: 10.1002/ajmg.a.36365

  7. A Pascual 1 Roman Amphora from Catalonia from the sea at Saint Alban's Head Ledge, Dorset, England

    International Journal of Nautical Archaeology

    Volume 42, Issue 1, March 2013, Pages: 193–196, D. Parham and A. P. Fitzpatrick

    Article first published online : 4 FEB 2013, DOI: 10.1111/j.1095-9270.2012.00368.x

  8. High-resolution Imaging of the M/SDodekanisosShipwreck Site off Deveboynu Burnu, Turkey

    International Journal of Nautical Archaeology

    Volume 42, Issue 1, March 2013, Pages: 204–208, Michael L. Brennan

    Article first published online : 4 FEB 2013, DOI: 10.1111/j.1095-9270.2012.00367.x

  9. Screening and familial characterization of copy-number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failure

    American Journal of Medical Genetics Part A

    Volume 161, Issue 10, October 2013, Pages: 2487–2494, Steven M. Harrison, Ian M. Campbell, Melise Keays, Candace F. Granberg, Carlos Villanueva, Grace Tannin, Andrew R. Zinn, Diego H. Castrillon, Chad A. Shaw, Pawel Stankiewicz and Linda A. Baker

    Article first published online : 5 AUG 2013, DOI: 10.1002/ajmg.a.36084

  10. Further insight into the phenotype associated with a mutation in the ORC6 gene, causing Meier–Gorlin syndrome 3

    American Journal of Medical Genetics Part A

    Volume 167, Issue 3, March 2015, Pages: 607–611, Stavit Allon Shalev, Morad Khayat, Daniel-Spiegl Etty and Orly Elpeleg

    Article first published online : 18 FEB 2015, DOI: 10.1002/ajmg.a.36906

  11. Hemiconvulsion–hemiplegia–epilepsy syndrome with 1q44 microdeletion: Causal or chance association

    American Journal of Medical Genetics Part A

    Volume 164, Issue 1, January 2014, Pages: 186–189, Rekha Gupta, Meenal Agarwal, Vijay R. Boqqula, Rajendra V. Phadke and Shubha R. Phadke

    Article first published online : 8 NOV 2013, DOI: 10.1002/ajmg.a.36198

  12. Microdeletion of 12q24.31: Report of a girl with intellectual disability, stereotypies, seizures and facial dysmorphisms

    American Journal of Medical Genetics Part A

    Volume 167, Issue 2, February 2015, Pages: 438–444, Orazio Palumbo, Pietro Palumbo, Maurizio Delvecchio, Teresa Palladino, Raffaella Stallone, Matteo Crisetti, Leopoldo Zelante and Massimo Carella

    Article first published online : 26 NOV 2014, DOI: 10.1002/ajmg.a.36872

  13. Evaluating the frequency and characteristics of seizures in 142 Japanese patients with prader–willi syndrome

    American Journal of Medical Genetics Part A

    Volume 161, Issue 8, August 2013, Pages: 2052–2055, Eri Takeshita, Nobuyuki Murakami, Ryoichi Sakuta and Toshiro Nagai

    Article first published online : 3 JUL 2013, DOI: 10.1002/ajmg.a.36015

  14. A 3p interstitial deletion in two monozygotic twin brothers and an 18-year-old man: Further characterization and review

    American Journal of Medical Genetics Part A

    Volume 161, Issue 10, October 2013, Pages: 2634–2640, Eva Maria Christina Schwaibold, Barbara Zoll, Peter Burfeind, Elke Hobbiebrunken, Bernd Wilken, Rudolf Funke and Moneef Shoukier

    Article first published online : 15 AUG 2013, DOI: 10.1002/ajmg.a.36129

  15. Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria

    American Journal of Medical Genetics Part A

    Volume 161, Issue 9, September 2013, Pages: 2321–2326, Samantha J Turner, Michael S. Hildebrand, Susan Block, John Damiano, Michael Fahey, Sheena Reilly, Melanie Bahlo, Ingrid E. Scheffer and Angela T. Morgan

    Article first published online : 5 AUG 2013, DOI: 10.1002/ajmg.a.36055

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    Familial very long chain acyl-CoA dehydrogenase deficiency as a cause of neonatal sudden infant death: Improved survival by prompt diagnosis

    American Journal of Medical Genetics Part A

    Volume 167, Issue 1, January 2015, Pages: 211–214, Emmanuel Scalais, Jean Bottu, Ronald J. A. Wanders, Sacha Ferdinandusse, Hans R. Waterham and Linda De Meirleir

    Article first published online : 22 OCT 2014, DOI: 10.1002/ajmg.a.36803

  17. Is cardiac rhabdomyoma a feature of Birt Hogg Dubé syndrome?

    American Journal of Medical Genetics Part A

    Volume 167, Issue 4, April 2015, Pages: 802–804, Davide Bondavalli, Susan M White, Andrew Steer, Andreas Pflaumer and Ingrid Winship

    Article first published online : 5 FEB 2015, DOI: 10.1002/ajmg.a.36917

  18. Unusual isochromosome 5p marker chromosome

    American Journal of Medical Genetics Part A

    Volume 167, Issue 2, February 2015, Pages: 455–459, Fanny Roulet-Coudrier, Amine Rouibi, Clotilde Thuillier, Sylvie Bourthoumieu, Aziza Lebbar, Jean-Michel Dupont and Catherine Yardin

    Article first published online : 25 NOV 2014, DOI: 10.1002/ajmg.a.36843

  19. Long term follow-up in a patient with a de novo microdeletion of 14q11.2 involving CHD8

    American Journal of Medical Genetics Part A

    Volume 167, Issue 4, April 2015, Pages: 837–841, Jana Drabova, Eva Seemanova, Miroslava Hancarova, Radka Pourova, Martin Horacek, Tereza Jancuskova, Sona Pekova, Drahuse Novotna and Zdenek Sedlacek

    Article first published online : 3 MAR 2015, DOI: 10.1002/ajmg.a.36957

  20. Expanding the phenotypic spectrum in EP300-related Rubinstein–Taybi syndrome

    American Journal of Medical Genetics Part A

    Volume 167, Issue 5, May 2015, Pages: 1111–1116, Benjamin D. Solomon, Dale L. Bodian, Alina Khromykh, Gabriela Gomez Mora, Brendan C. Lanpher, Ramaswamy K. Iyer, Rajiv Baveja, Joseph G. Vockley and John E. Niederhuber

    Article first published online : 25 FEB 2015, DOI: 10.1002/ajmg.a.36883