American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

1 July 1992

Volume 43, Issue 4

Pages fmi–fmi, 651–768

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Appreciation
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Erratum
    1. Masthead (page fmi)

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430401

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Appreciation
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Erratum
    1. Encephalocraniocutaneous lipomatosis and the Proteus syndrome: Distinct entities with overlapping manifestations (pages 662–668)

      Sherman McCall, Magda I. Ramzy, Joel K. Cure and Dr. G. S. Pai

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430403

    2. New multiple congenital anomalies: Mental retardation syndrome (MCA/MR) with facio-cutaneous-skeletal involvement (pages 678–685)

      Zvi Borochowitz, Lorenzo Pavone, Galia Mazor, Renata Rizzo and Hanna Dar

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430405

    3. Bilateral anophthalmia, esophageal atresia, and right cryptorchidism: A new entity? (pages 686–687)

      Dr. Ignacio Arroyo, María Jesús García, Carmen Eloína Cimadevilla, Valentín Carretero, Eva Bermejo and María Luisa Martínez-Frías

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430406

    4. Craniosynostosis associated with partial duplication of 15q and deletion of 2q (pages 688–692)

      M. I. Van Allen, J. Siegel-Bartelt, A. Feigenbaum and I. E. Teshima

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430407

  3. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Appreciation
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Erratum
    1. Nail-Patella syndrome in a spontaneously aborted 18-week fetus: Ultrastructural and immunofluorescent study of the kidneys (pages 693–696)

      Rosa Monica Drut, Sunita Chandra, Rocco Latorraca and Dr. Enid Gilbert-Barness

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430408

    2. Trisomy 9: An additional case with unique manifestations (pages 697–700)

      Dr. María I. de Michelena, Raul Sánchez, Pedro Muñoz, Emilio Cabello, Pablo Rojas and Eduardo de Olazaval

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430409

  4. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Appreciation
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Erratum
    1. Interstitial deletion of 10q: Clinical features and literature review (pages 701–703)

      Sandra Lobo, Jaroslav Cervenka, Arnold London and Mary Ella M. Pierpont

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430410

    2. Cervical spine in the Apert syndrome (pages 704–708)

      Sven Kreiborg, Mason Barr Jr. and Dr. M. Michael Cohen Jr.

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430411

    3. Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes (pages 709–715)

      Dr. D. F. Callen, H. Eyre, M-Y. Yip, J. Freemantle and E. A. Haan

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430412

    4. Pigmentary dysplasias and chromosomal mosaicism: Report of 9 cases (pages 716–721)

      Hirofumi Ohashi, Masato Tsukahara, Ichiro Murano, Kenji Naritomi, Kazue Nishioka, Susumu Miyake and Tadashi Kajii

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430413

    5. Joubert syndrome: A review (pages 726–731)

      Jorge M. Saraiva and Dr. Michael Baraitser

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430415

    6. Craniorachischisis totalis and sirenomelia (pages 732–736)

      Dr. José Ignacio Rodríguez and José Palacios

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430416

  5. Appreciation

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Appreciation
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Erratum
    1. You have free access to this content
      Hans-Rudolf Wiedemann: An appreciation (pages 737–739)

      John M. Opitz and Pierce Mullen

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430417

  6. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Appreciation
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Erratum
    1. Living history-autobiography: Hans-Rudolf Wiedemann in a half century of german pediatric genetics (pages 740–746)

      Prof. Dr. med. Drs. med. h.c. Hans-Rudolf Wiedemann

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430418

    2. Two patients with chromosome 6q terminal deletions with breakpoints at q24.3 and q25.3 (pages 747–750)

      Jianguo Meng, Dr. Hiroko Fujita, Noboru Nagahara, Akira Kashiwai, Yasushi Yoshioka and Masahisa Funato

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430419

  7. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Appreciation
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Erratum
    1. Paraplegia and congenital contractures as a consequence of intrauterine trauma (pages 751–752)

      Leah K. Weyerts, Marilyn C. Jones and Hector E. James

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430420

  8. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Appreciation
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Erratum
    1. Terminal deletion of chromosome 4p (4p16.3) shows a breakpoint between loci linked to Huntington disease (pages 753–758)

      Dr. Elina Ikonen, Armi Salo, Mirja Somer, Hannu Somer, Leena Pääkkönen and Leena Peltonen

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430421

    2. Trisomy 18 and a constitutional maternal translocation (2;18) (pages 759–761)

      Ikuko E. Teshima, Elizabeth J. T. Winsor and Margot I. Van Allen

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430422

    3. Familial aplasia cutis congenita and coarctation of the aorta (pages 762–763)

      B. Dallapiccola, A. Giannotti, B. Marino, C. Digilio and G. Obregon

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430423

    4. Albright hereditary osteodystrophy with hypothyroidism, normocalcemia, and normal Gs protein activity: A family presenting with congenital osteoma cutis (pages 764–767)

      Shai Izraeli, Aryeh Metzker, Gadi Horev, Doron Karmi, Paul Merlob and Zvi Farfel

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430424

  9. Erratum

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Appreciation
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Erratum
    1. You have free access to this content

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