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There are 7884316 results for: content related to: Corrigendum to “Hyperphosphatasia With Seizures, Neurologic Deficit, and Characteristic Facial Features: Five New Patients With Mabry Syndrome” Am J Med Genet 152A: 1661-1669

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    American Journal of Medical Genetics Part A: Volume 152A, Number 5, May 2010

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 5, May 2010, Page: C1,

    Version of Record online : 22 APR 2010, DOI: 10.1002/ajmg.a.33500

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    Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome)

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 3, March 2012, Pages: 553–558, Miles D. Thompson, Tony Roscioli, Carlo Marcelis, Marjan M. Nezarati, Irene Stolte-Dijkstra, Frances J. Sharom, Peihua Lu, John A. Phillips, Elizabeth Sweeney, Peter N. Robinson, Peter Krawitz, Helger G. Yntema, Danielle M. Andrade, Han G. Brunner and David E.C. Cole

    Version of Record online : 7 FEB 2012, DOI: 10.1002/ajmg.a.35202

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    Erratum to “Longitudinal Observation of a Patient With Rieger Syndrome and Interstitial Deletion 4 (q25–q31.1)” [Am J Med Genet Part A 152A:977–981]

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 6, June 2010, Pages: 1602–1603, Lilia Moreira, Albert Schinzel, Alessandra Baumer, Paula Pinto, Fátima Góes, Maria de Lourdes Falcao, Ana Luiza Barbosa and Mariluce Riegel

    Version of Record online : 20 MAY 2010, DOI: 10.1002/ajmg.a.33467

  4. Hyperphosphatasia with seizures, neurologic deficit, and characteristic facial features: Five new patients with Mabry syndrome

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 7, July 2010, Pages: 1661–1669, Miles D. Thompson, Marjan M. Nezarati, Gabriele Gillessen-Kaesbach, Peter Meinecke, Roberto Mendoza, Etienne Mornet, Isabelle Brun-Heath, Catherine Prost Squarcioni, Laurence Legeai-Mallet, Arnold Munnich and David E.C. Cole

    Version of Record online : 3 JUN 2010, DOI: 10.1002/ajmg.a.33438

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    Corrigendum to “Overview of German, Nazi, and Holocaust Medicine. Am J Med Genet 152A:687–707, 2010”

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 1, January 2012, Page: 266, M. Michael Cohen Jr

    Version of Record online : 21 DEC 2011, DOI: 10.1002/ajmg.a.34323

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    Erratum to: An Interstitial 15q11–q14 Deletion: Expanded Prader–Willi Syndrome Phenotype (DOI 10.1002/ajmg.a.33197; Am J Med Genet Part A 152A:404–408)

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 5, May 2010, Pages: 1331–1332, Merlin G. Butler, Douglas C. Bittel, Nataliya Kibiryeva, Linda D. Cooley and Shihui Yu

    Version of Record online : 22 APR 2010, DOI: 10.1002/ajmg.a.33403

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    Table of Contents, Volume 152A, Number 5, May 2010

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 5, May 2010, Pages: fm i–fm v,

    Version of Record online : 22 APR 2010, DOI: 10.1002/ajmg.a.33501

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    Appendix B: Syntax Reference

    VHDL for Logic Synthesis, Third Edition

    Andrew Rushton, Pages: 439–447, 2011

    Published Online : 26 APR 2011, DOI: 10.1002/9781119995852.app2

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    American Journal of Medical Genetics Part A: Volume 152A, Number 2, February 2010

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 2, February 2010, Page: C1,

    Version of Record online : 25 JAN 2010, DOI: 10.1002/ajmg.a.33350

  10. Hereditary multiple exostoses with spine involvement in a 4-year-old boy

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 5, May 2010, Page: 1263, James W. Roach

    Version of Record online : 13 APR 2010, DOI: 10.1002/ajmg.a.33354

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    Journal of Cellular Biochemistry: Volume 112, Number 5, May, 2011

    Journal of Cellular Biochemistry

    Volume 112, Issue 5, May 2011, Page: C1,

    Version of Record online : 4 APR 2011, DOI: 10.1002/jcb.23133

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    Features: Volume 112, Number 5

    Journal of Cellular Biochemistry

    Volume 112, Issue 5, May 2011, Pages: fm iv–fm v,

    Version of Record online : 4 APR 2011, DOI: 10.1002/jcb.22812

  13. Book review

    American Journal of Medical Genetics Part A

    Volume 155, Issue 5, May 2011, Page: 1212, F. Clarke Fraser

    Version of Record online : 4 APR 2011, DOI: 10.1002/ajmg.a.33973

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    In this issue

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 3, March 2012, Page: x,

    Version of Record online : 16 FEB 2012, DOI: 10.1002/ajmg.a.35282

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    American Journal of Medical Genetics Part A: Volume 155, Number 5, May 2011

    American Journal of Medical Genetics Part A

    Volume 155, Issue 5, May 2011, Page: C1,

    Version of Record online : 19 APR 2011, DOI: 10.1002/ajmg.a.34092

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    American Journal of Medical Genetics Part A: Volume 152A, Number 10, October 2010

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 10, October 2010, Page: C1,

    Version of Record online : 21 SEP 2010, DOI: 10.1002/ajmg.a.33731

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    American Journal of Medical Genetics Part A: Volume 152A, Number 8, August 2010

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 8, August 2010, Page: C1,

    Version of Record online : 21 JUL 2010, DOI: 10.1002/ajmg.a.33661

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    Table of Contents, Volume 152A, Number 7, July 2010

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 7, July 2010, Pages: fm i–fm v,

    Version of Record online : 25 JUN 2010, DOI: 10.1002/ajmg.a.33603

  19. Relative rate constants for reactions of HFC 152a, 143, 143a, 134a, and HCFC 124 with F or Cl atoms and for CF2CH3, CF2HCH2, and CF3CFH radicals with F2, Cl2, and O2

    International Journal of Chemical Kinetics

    Volume 25, Issue 8, August 1993, Pages: 667–680, E. W. Kaiser

    Version of Record online : 30 SEP 2004, DOI: 10.1002/kin.550250807

  20. Saturated liquid thermal conductivity correlations for some new refrigerants

    International Journal of Energy Research

    Volume 22, Issue 6, May 1998, Pages: 579–590, K. Srinivasan and L. R. Oellrich

    Version of Record online : 4 DEC 1998, DOI: 10.1002/(SICI)1099-114X(199805)22:6<579::AID-ER387>3.0.CO;2-U