American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

September 1987

Volume 28, Issue 1

Pages fmi–fmi, 1–260

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. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
    1. Masthead (page fmi)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320280101

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
    1. Individual variation and specific cognitive deficits in the fra(X) syndrome (pages 1–11)

      Theresa M. Theobald, Dr. David A. Hay, Cliff Judge and John M. Opitz

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280102

    2. Invited editorial comment: Cognitive variability in the fragile X syndrome (pages 13–15)

      Dr. Albert E. Chudley, Robert de von Flindt and Randi J. Hagerman

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280103

    3. Neu-Laxova syndrome: Report of a case and comments (pages 17–23)

      Dr. Mohammad Hassan Karimi-Nejad, Hooshang Khajavi, Mohammad Jafar Gharavi, Roxana Karimi-Nejad, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280104

    4. A genetic follow-up study of 64 patients with the Pierre Robin complex (pages 25–36)

      Dr. L. J. Sheffield, J. A. Reiss, K. Strohm, M. Gilding, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280105

    5. Familial Prader-Willi syndrome with apparently normal chromosomes (pages 37–43)

      Mark Lubinsky, Hans Zellweger, Louise Greenswag, Gary Larson, Irving Hansmann, David Ledbetter, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280106

    6. Clinical heterogeneity associated with deletions in the long arm of chromosome 15: Report of 3 new cases and their possible genetic significance (pages 45–53)

      Dr. Lawrence C. Kaplan, Robert Wharton, Ellen Elias, Frederick Mandell, Timothy Donlon, Samuel A. Latt, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280107

  3. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
    1. Atypical phenotype associated with deletion (15) (pter [RIGHTWARDS ARROW] q11::q13 [RIGHTWARDS ARROW] qter) (pages 55–58)

      Dr. James F. Reynolds, Art Daniel, Joan FitzGerald and John M. Opitz

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280108

  4. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
    1. Recurrence risk in Prader-Willi syndrome (pages 59–60)

      Dr. Suzanne B. Cassidy, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280109

  5. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
    1. Cyclopia and congenital cytomegalovirus infection (pages 61–65)

      Dr. Paul J. Byrne, Meredith M. Silver, Joseph M. Gilbert, Werner Cadera, A. Keith Tanswell and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280110

  6. Invited Editorial Essay

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
    1. Twinning, nonrighthandedness, and fusion malformations: Evidence for heritable causal elements held in common (pages 67–84)

      Charles E. Boklage, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320280111

  7. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
    1. Diprosopus with associated malformations: Report of two cases (pages 85–88)

      Lorenzo Pavone, Gianni Camera, Sebastiano Grasso, Claudio Gambini, Mauro Barberis, Salvo Garaffo, Sebastiano Russo and Giovanni Neri

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280112

  8. Invited Editorial Comment

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
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      Lessons from conjoined twins (pages 89–97)

      Dr. G. A. Machin, G. H. Sperber, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280113

  9. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
    1. Monozygosity and holoprosencephaly: Cleavage disorders of the “midline field” (pages 99–102)

      Lorraine Suslak, Gaines M. Mimms, Franklin Desposito, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280114

  10. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
    1. Goldenhar complex in discordant monozygotic twins: A case report and review of the literature (pages 103–109)

      Debra J. Boles, Joann Bodurtha, Walter E. Nance and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280115

    2. X-linked laterality sequence: Situs inversus, complex cardiac defects, splenic defects (pages 111–116)

      Robert S. Mathias, Ronald V. Lacro, Dr. Kenneth Lyons Jones, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280116

    3. Thrombocytopenia with absent radius in a boy and his uncle (pages 117–123)

      Dr. Rhonda E. Schnur, Deborah L. Eunpu, Elaine H. Zackai, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280117

    4. Follow-up on seven adult patients with mild Sanfilippo B-disease (pages 125–129)

      H. M. J. Van Schrojenstein-de Valk, Dr. J. J. P. van de Kamp and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320280118

    5. Renal insufficiency in Williams syndrome (pages 131–135)

      Leslie G. Biesecker, Dr. Renata Laxova, Aaron Friedman and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280119

  11. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
    1. Syndrome of osteopetrosis and muscular degeneration associated with cerebro-oculo-facio-skeletal changes (pages 137–142)

      Dr. Tally Lerman-Sagie, Yael Levi, Deborah Kidron, Michael Grünebaum, Menachem Nitzan, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320280120

  12. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
    1. Gonadal mosaicism in pseudoachondroplasia (pages 143–151)

      Dr. Judith G. Hall, John P. Dorst, Julie Rotta, Victor A. McKusick, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280121

    2. Apparent Apert syndrome with polydactyly: Rare pleiotropic manifestation or new syndrome? (pages 153–158)

      Pierre Maroteaux, Marie Christine Fonfria, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280122

    3. Recurrence risks in the presence of single gene susceptibility to environmental agents (pages 159–169)

      Dr. Muin J. Khoury, Terri H. Beaty, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280123

    4. Neuroaxonal dystrophy presenting with neonatal dysmorphic features, early onset of peripheral gangrene, and a rapidly lethal course (pages 171–180)

      Dr. Alasdair G. W. Hunter, Carmencita L. Jimenez, Blair F. Carpenter, Ian MacDonald, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280124

    5. Uncombable hair (pili trianguli et Canaliculi): Evidence for dominant inheritance with complete penetrance based on scanning electron microscopy (pages 185–193)

      Adelaide A. Hebert, Dr. Joel Charrow, Nancy B. Esterly, David F. Fretzin, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280126

    6. Further delineation of the 3-M syndrome with review of the literature (pages 195–209)

      Raoul C. M. Hennekam, Jan B. Bijlsma, Jürgen Spranger and Giovanni Neri

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280127

    7. Decreased superoxide dismutase-2 activity in a patient with ring chromosome 6 (pages 211–214)

      Dr. Kazunori Yoshimitsu, Yoshikazu Nishi, Yohnosuke Kobayashi, Osamu Yoshimura, Koso Ohama, Nobuo Oguma, Tomofusa Usui, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280128

  13. Editorial Comment

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
    1. Lester Casida (page 215)

      Dr. John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320280129

  14. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
    1. Memorial resolution of the faculty of the university of Wisconsin-Madison on the death of emeritus Professor Lester Earl Casida (pages 217–219)

      Neal L. First, Oliver J. Ginther, Edward R. Hauser, Charles A. Kiddy and Arthur B. Chapman

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320280130

    2. To the editor (page 221)

      Dr. Marion S. Verp, Anthony P. Amarose and John M. Opitz

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280131

    3. To the editor (page 223)

      Wilson Hwei-Yuen Lo

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320280132

  15. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
    1. Familial situs inversus and congenital heart defects (pages 227–228)

      Andrew Czeizel, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320280134

    2. Normal high-resolution karyotypes in three patients with the Holt-Oram syndrome (pages 229–231)

      Ulf Kristoffersson, Anita Mineur, Sverre Heim, Nils Mandahl, Felix Mitelman and Giovanni Neri

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280135

  16. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Letter to the Editor
    6. Articles
    7. Invited Editorial Essay
    8. Articles
    9. Invited Editorial Comment
    10. Letter to the Editor
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Editorial Comment
    15. Articles
    16. Letter to the Editor
    17. Articles
    1. A nonpathologic allele (IW) for low α-L-iduronidase enzyme activity vis-a-vis prenatal diagnosis of Hurler syndrome (pages 233–243)

      Chester B. Whitley, Robert J. Gorlin, William Krivit, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320280136

    2. Close linkage of the Wieacker-Wolff syndrome to the DNA segment DXYS1 in proximal Xq (pages 245–253)

      Peter Wieacker, Gerhard Wolff, Thomas F. Wienker, John M. Opitz and James F. Reynolds

      Version of Record online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280137

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