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There are 7052420 results for: content related to: Corrigendum to: “Myopathy in a 20-Year-Old Female Patient With D4ST-1 Deficient Ehlers-Danlos Syndrome Due to a Homozygous CHST14 Mutation, Am J Med Genet A. 2012 Apr; 158A(4):850–855”

  1. Myopathy in a 20-year-old female patient with D4ST-1 deficient Ehlers-Danlos syndrome due to a homozygous CHST14 mutation

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 4, April 2012, Pages: 850–855, N.C. Voermans, M. Kempers, M. Lammens, N. van Alfen, M.C. Janssen, C. Bönnemann, B.G. van Engelen and B.C. Hamel

    Version of Record online : 9 MAR 2012, DOI: 10.1002/ajmg.a.35232

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    American Journal of Medical Genetics Part A: Volume 158A, Number 6, June 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 6, June 2012, Page: C1,

    Version of Record online : 17 MAY 2012, DOI: 10.1002/ajmg.a.35510

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    American Journal of Medical Genetics Part A: Volume 158A, Number 7, July 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 7, July 2012, Page: C1,

    Version of Record online : 18 JUN 2012, DOI: 10.1002/ajmg.a.35543

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    American Journal of Medical Genetics Part A: Volume 158A, Number 5, May 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 5, May 2012, Page: C1,

    Version of Record online : 19 APR 2012, DOI: 10.1002/ajmg.a.35451

  5. The neuromuscular differential diagnosis of joint hypermobility

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

    Volume 169, Issue 1, March 2015, Pages: 23–42, S. Donkervoort, C.G. Bonnemann, B. Loeys, H. Jungbluth and N.C. Voermans

    Version of Record online : 26 MAR 2015, DOI: 10.1002/ajmg.c.31433

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    Table of Contents, Volume 158A, Number 4, April 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 4, April 2012, Pages: fm i–fm v,

    Version of Record online : 26 MAR 2012, DOI: 10.1002/ajmg.a.35404

  7. Observations of double stars

    Astronomische Nachrichten

    Volume 182, Issue 16, 1909, Pages: 253–272, Charles P. Olivier, Ralph E. Wilson and W. Newton

    Version of Record online : 23 MAR 2006, DOI: 10.1002/asna.19091821602

  8. The ETFDH c.158A>G Variation Disrupts the Balanced Interplay of ESE- and ESS-Binding Proteins thereby Causing Missplicing and Multiple Acyl-CoA Dehydrogenation Deficiency

    Human Mutation

    Volume 35, Issue 1, January 2014, Pages: 86–95, Rikke K. J. Olsen, Sabrina Brøner, Rugivan Sabaratnam, Thomas K. Doktor, Henriette S. Andersen, Gitte H. Bruun, Birthe Gahrn, Vibeke Stenbroen, Simon E. Olpin, Angus Dobbie, Niels Gregersen and Brage S. Andresen

    Version of Record online : 28 OCT 2013, DOI: 10.1002/humu.22455

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    American Journal of Medical Genetics Part A: Volume 158A, Number 11, November 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Page: C1,

    Version of Record online : 18 OCT 2012, DOI: 10.1002/ajmg.a.35744

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    American Journal of Medical Genetics Part A: Volume 158A, Number 8, August 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 8, August 2012, Page: C1,

    Version of Record online : 20 JUL 2012, DOI: 10.1002/ajmg.a.35605

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    American Journal of Medical Genetics Part A: Volume 158A, Number 4, April 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 4, April 2012, Page: C1,

    Version of Record online : 26 MAR 2012, DOI: 10.1002/ajmg.a.35403

  12. Management of pain and fatigue in the joint hypermobility syndrome (a.k.a. Ehlers–Danlos syndrome, hypermobility type): Principles and proposal for a multidisciplinary approach

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 8, August 2012, Pages: 2055–2070, Marco Castori, Silvia Morlino, Claudia Celletti, Mauro Celli, Aldo Morrone, Marina Colombi, Filippo Camerota and Paola Grammatico

    Version of Record online : 11 JUL 2012, DOI: 10.1002/ajmg.a.35483

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    American Journal of Medical Genetics Part A: Volume 158A, Number 2, February 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 2, February 2012, Page: C1,

    Version of Record online : 20 JAN 2012, DOI: 10.1002/ajmg.a.35252

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    American Journal of Medical Genetics Part A: Volume 158A, Number 12, December 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 12, December 2012, Page: C1,

    Version of Record online : 22 NOV 2012, DOI: 10.1002/ajmg.a.35806

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    American Journal of Medical Genetics Part A: Volume 158A, Number 9, September 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 9, September 2012, Page: C1,

    Version of Record online : 24 AUG 2012, DOI: 10.1002/ajmg.a.35648

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    American Journal of Medical Genetics Part A: Volume 158A, Number 10, October 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 10, October 2012, Page: C1,

    Version of Record online : 19 SEP 2012, DOI: 10.1002/ajmg.a.35688

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    American Journal of Medical Genetics Part A: Volume 158A, Number 3, March 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 3, March 2012, Page: C1,

    Version of Record online : 16 FEB 2012, DOI: 10.1002/ajmg.a.35324

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    American Journal of Medical Genetics Part A: Volume 158A, Number 1, January 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 1, January 2012, Page: C1,

    Version of Record online : 21 DEC 2011, DOI: 10.1002/ajmg.a.35218

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    Table of Contents, Volume 161A, Number 2, February 2013

    American Journal of Medical Genetics Part A

    Volume 161, Issue 2, February 2013, Pages: fm i–fm iv,

    Version of Record online : 24 JAN 2013, DOI: 10.1002/ajmg.a.35891

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    Table of Contents, Volume 158A, Number 11, November 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: fm i–fm vi,

    Version of Record online : 18 OCT 2012, DOI: 10.1002/ajmg.a.35745