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There are 19158 results for: content related to: Are stepfathers’ education levels associated with the intelligence of their stepsons? A register-based study of Norwegian half-brothers

  1. When brother–sister marriage becomes incest

    The Australian Journal of Anthropology

    Volume 21, Issue 2, August 2010, Pages: 228–245, Grant Evans

    Article first published online : 17 AUG 2010, DOI: 10.1111/j.1757-6547.2010.00080.x

  2. A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome

    American Journal of Medical Genetics

    Volume 29, Issue 2, February 1988, Pages: 419–423, Dr. Stephen Wood, Robert J. Shukin, Barbara C. McGillivray, Peter N. Ray, Ronald G. Worton, John M. Optiz and James F. Reynolds

    Article first published online : 3 JUN 2005, DOI: 10.1002/ajmg.1320290225

  3. Characterization of a familial balanced rec(13) in a child with mild MR and his half-sibling with two structurally rearranged chromosomes 13

    American Journal of Medical Genetics Part A

    Volume 137A, Issue 2, 30 August 2005, Pages: 217–221, S. Mehra, L. Christ, L. Jeng, A. B. Zinn and S. Schwartz

    Article first published online : 29 JUL 2005, DOI: 10.1002/ajmg.a.30866

  4. Low-Income Mothers as “Othermothers” to Their Romantic Partners' Children: Women's Coparenting in Multiple Partner Fertility Relationships

    Family Process

    Volume 51, Issue 3, September 2012, Pages: 343–359, Linda M. Burton and Cecily R. Hardaway

    Article first published online : 17 SEP 2012, DOI: 10.1111/j.1545-5300.2012.01401.x

  5. Moderate hemophilia B leyden: Identification by polymerase chain reaction, sequencing, and oligomer restriction

    American Journal of Hematology

    Volume 46, Issue 3, July 1994, Pages: 234–240, Dr. Thomas E. Coyle, Timothy Spicer, Doris Michalovic and Bernard J. Poiesz

    Article first published online : 11 JUL 2006, DOI: 10.1002/ajh.2830460314

  6. Two Novel Mutations in ABHD12: Expansion of the Mutation Spectrum in PHARC and Assessment of Their Functional Effects

    Human Mutation

    Volume 34, Issue 12, December 2013, Pages: 1672–1678, Dong-Hui Chen, Alipi Naydenov, Jacqueline L. Blankman, Heather C. Mefford, Marie Davis, Youngmee Sul, A. Samuel Barloon, Emily Bonkowski, John Wolff, Mark Matsushita, Corrine Smith, Benjamin F. Cravatt, Ken Mackie, Wendy H. Raskind, Nephi Stella and Thomas D. Bird

    Article first published online : 2 OCT 2013, DOI: 10.1002/humu.22437

  7. Creatine transporter deficiency in two half-brothers

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 8, August 2010, Pages: 1979–1983, Orly Ardon, Cristina Amat di San Filippo, Gajja S. Salomons and Nicola Longo

    Article first published online : 2 JUL 2010, DOI: 10.1002/ajmg.a.33551

  8. Transmission of the fra(X) haplotype from three nonpenetrant brothers to their affected grandsons

    American Journal of Medical Genetics

    Volume 43, Issue 3, 1 June 1992, Pages: 588–591, A. J. Kirkilionis, A. E. Chudley, C. R. Greenberg, D. L. Yan, B. McGillivray and J. L. Hamerton

    Article first published online : 7 JUN 2005, DOI: 10.1002/ajmg.1320430316

  9. A Clotting Defect in an Arab Colt Foal

    Equine Veterinary Journal

    Volume 9, Issue 1, January 1977, Pages: 1–3, M. Hinton, D. R. E. Jones, I. M. LEWIS and Patricia E. Thomson

    Article first published online : 23 APR 2010, DOI: 10.1111/j.2042-3306.1977.tb03959.x

  10. Identification of a dup(5)(p15.3) by multicolor banding

    Clinical Genetics

    Volume 61, Issue 4, April 2002, Pages: 277–282, D Riordan, A Vust, DE Wickstrom, J Brown, AE Chudley, D Tomkins, I Chudoba and AJ Dawson

    Article first published online : 27 MAY 2002, DOI: 10.1034/j.1399-0004.2002.610406.x

  11. Serologic evidence that factor IX inhibitor in the plasma of hemophilia B patients detects factor IX on normal red cells


    Volume 36, Issue 5, May 1996, Pages: 467–469, J. L. Swanson, C. L. Moertel, D. F. Stroncek and N. S. Key

    Article first published online : 28 FEB 2003, DOI: 10.1046/j.1537-2995.1996.36596282593.x

  12. A t(5;16)(p15.32;q23.3) generating 16q23.3 [RIGHTWARDS ARROW] qter duplication and 5p15.32 [RIGHTWARDS ARROW] pter deletion in two siblings with mental retardation, dysmorphic features, and speech delay

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 6, June 2010, Pages: 1555–1560, Ali Hellani, Sarar Mohamed, Siham Al-Akoum, Thomas M. Bosley and Khaled K. Abu-Amero

    Article first published online : 14 MAY 2010, DOI: 10.1002/ajmg.a.33400

  13. Familial plantar fibromatosis

    Journal of Surgical Oncology

    Volume 29, Issue 4, August 1985, Pages: 240–241, Karl T. K. Chen and Timothy A. Van Dyne

    Article first published online : 19 JUL 2006, DOI: 10.1002/jso.2930290410

  14. Duplication and deletion of chromosome band 2(p21p22) resulting from a familial interstitial insertion (2;11)(p21;p15)

    American Journal of Medical Genetics

    Volume 49, Issue 4, 15 February 1994, Pages: 422–427, Jeffrey R. Sawyer, Emmett Jones, Flora F. Hawks, J. Gerald Quirk Jr. and Christopher Cunniff

    Article first published online : 7 JUN 2005, DOI: 10.1002/ajmg.1320490414

  15. You have free access to this content
    Exome sequencing reveals FAM20c mutations associated with fibroblast growth factor 23–related hypophosphatemia, dental anomalies, and ectopic calcification

    Journal of Bone and Mineral Research

    Volume 28, Issue 6, June 2013, Pages: 1378–1385, Silje Hjorth Rafaelsen, Helge Ræder, Anne Kristine Fagerheim, Per Knappskog, Thomas O Carpenter, Stefan Johansson and Robert Bjerknes

    Article first published online : 21 MAY 2013, DOI: 10.1002/jbmr.1850

  16. Pigmentary mosaicism of the hyperpigmented type in two half-brothers

    American Journal of Medical Genetics

    Volume 112, Issue 1, 15 September 2002, Pages: 65–69, Denise Horn, Rudolf Happle, Heidemarie Neitzel and Jürgen Kunze

    Article first published online : 28 JUN 2002, DOI: 10.1002/ajmg.10600

  17. A Possible D(CW) (e) Gene Complex of the Rh System

    Vox Sanguinis

    Volume 25, Issue 5, November 1973, Pages: 385–389, Leif Kornstad and Anna M. Heier Larsen

    Article first published online : 5 MAR 2009, DOI: 10.1111/j.1423-0410.1973.tb03529.x

  18. You have free access to this content
    Induction of the Acrosome Reaction and Zona-Free Hamster Oocyte Penetration by a Bull With Complete Teratospermia Versus a Half Brother With Normal Sperm

    Journal of Andrology

    Volume 23, Issue 1, January-February 2002, Pages: 98–106, SHELLEY R. HOUGH, MICHAEL T. KAPROTH and ROBERT H. FOOTE Dr

    Article first published online : 2 JAN 2013, DOI: 10.1002/j.1939-4640.2002.tb02602.x


    Acta Psychiatrica Scandinavica

    Volume 26, Issue S69, May 1951, Pages: 59–110,

    Article first published online : 23 AUG 2007, DOI: 10.1111/j.1600-0447.1951.tb04191.x

  20. Familial congenital diaphragmatic defects: Aspects of etiology, prenatal diagnosis, and treatment

    American Journal of Medical Genetics

    Volume 17, Issue 2, February 1984, Pages: 471–483, Dr. Reijo Norio, Helena Kääriäinen, Juhani Rapola, Ritta Herva and Martti Kekomäki

    Article first published online : 6 JUN 2005, DOI: 10.1002/ajmg.1320170210