American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

September 1988

Volume 31, Issue 1

Pages fmi–fmi, 1–252

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Brief Clinical Report
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Letter to the Editors
    8. Rapid Publication Articles
    9. Editorial Policy
    1. You have free access to this content
      Masthead (page fmi)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320310101

  2. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Brief Clinical Report
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Letter to the Editors
    8. Rapid Publication Articles
    9. Editorial Policy
    1. Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomaly (pages 1–4)

      Dr. Frank Greenberg, Kristine B. Courtney, Robert A. Wessels, Dr. James Huhta, Robert J. Carpenter, Donna C. Rich, David H. Ledbetter, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310102

  3. Articles

    1. Top of page
    2. Masthead
    3. Brief Clinical Report
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Letter to the Editors
    8. Rapid Publication Articles
    9. Editorial Policy
    1. Pregnancy in women with cerebrotendinous xanthomatosis (CTX): High risk condition for fetus and newborn infant? (pages 11–16)

      V. M. Berginer, Dr. R. Carmi, G. Salen, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320310104

    2. Corpus callosum agenesis, facial anomalies, Robin sequence, and other anomalies: A new autosomal recessive syndrome? (pages 17–23)

      Dr. Helga V. Toriello, John C. Carey, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310105

    3. A new form of hypohidrotic ectodermal dysplasia (pages 25–32)

      Dr. Denis L. Viljoen, Williams S. Winship, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320310106

    4. Complex de novo rearrangement involving four chromosomes and ten break points with interstitial deletions and duplication (pages 33–37)

      Dr. Razia S. Muneer, Jeannie Himes, Owen M. Rennert, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310107

    5. Inherited lysosomal storage disease associated with deficiencies of β-galactosidase and α-neuraminidase in sheep (pages 39–56)

      Amelia J. Ahern-Rindell, Dr. David J. Prieur, Robert D. Murnane, Srinivasa S. Raghavan, Peter F. Daniel, Robert H. McCluer, Steven U. Walkley, Steven M. Parish, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310108

    6. Arachnodactyly and unusual dermatoglyphics: Study of a case (pages 57–62)

      Mrs. Anne J. Krush, Blanka A. Schaumann, Hagop Youssoufian, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310109

    7. Amnion rupture sequence in previable fetuses (pages 63–73)

      Dr. D. K. Kalousek, S. Bamforth, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320310110

    8. Congenital adrenal hypoplasia and selective absence of pituitary luteinizing hormone: A new autosomal recessive syndrome (pages 75–97)

      Dr. B. A. Burke, M. R. Wick, R. King, T. Thompson, J. Hansen, B. T. Darrae, U. Francke, W. K. Seltzer, E. R. B. McCabe, B. W. Scheithauer, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310111

    9. Congenital scalp defects with distal limb anomalies (Adams-Oliver syndrome): Report of ten cases and review of the literature (pages 99–115)

      Dr. Wolfgang Küster, Widukind Lenz, Helena Kääriäinen, Frank Majewski, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310112

  4. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Brief Clinical Report
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Letter to the Editors
    8. Rapid Publication Articles
    9. Editorial Policy
    1. Achondroplasia with ankylosing spondylitis (pages 117–121)

      Dr. L. M. Randolph, M. Shohat, D. Miller, R. Lachman, D. L. Rimoin, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310113

    2. Dandy-Walker malformation in Ellis-van Creveld syndrome (pages 123–129)

      Kenneth M. Zangwill, Danielle K. B. Boal, Dr. Roger L. Ladda, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320310114

  5. Articles

    1. Top of page
    2. Masthead
    3. Brief Clinical Report
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Letter to the Editors
    8. Rapid Publication Articles
    9. Editorial Policy
    1. Cohen syndrome: A connective tissue disorder? (pages 131–133)

      Prof. Károly Méhes, György Kosztolányi, Maria Kardos, Magdolna Horváth, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310115

    2. Familial dilated cardiomyopathy (pages 135–143)

      Michael A. Schmidt, Dr. Virginia V. Michels, William D. Edwards, Fletcher A. Miller, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310116

    3. Developmental delay, short stature, and minor facial anomalies in a child with ring chromosome 16 (pages 145–151)

      Bernard N. Chodirker, Manoranjan Ray, Phyllis J. McAlpine, Diane Riordan, Alice Vust, Dora Pugh, Dr. Albert E. Chudley, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310117

    4. Hypomagnesemia masking the appearance of elevated parathyroid hormone concentrations in familial pseudohypoparathyroidism (pages 153–158)

      Dr. David B. Allen, Aaron L. Friedman, Frank R. Greer, Russell W. Chesney, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320310118

    5. Fraser syndrome (cryptophthalmos-syndactyly syndrome): A review of eleven cases with postmortem findings (pages 159–168)

      P. A. Boyd, J. W. Keeling, R. H. Lindenbaum, Giovanni Neri and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310119

    6. Probable metachromatic leukodystrophy/pseudodeficiency compound heterozygote at the arylsulfatase A locus with neurological and psychiatric symptomatology (pages 169–175)

      Ch. Hohenschutz, W. Friedl, K.-H. Schlör, A. Waheed, E. Conzelmann, K. Sandhoff, Dr. P. Propping, Giovanni Neri and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310120

  6. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Brief Clinical Report
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Letter to the Editors
    8. Rapid Publication Articles
    9. Editorial Policy
    1. Parental coital rates and down syndrome (pages 177–178)

      William H. James, Giovanni Neri and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310121

    2. Recessive inheritance of apparent apart syndrome with polysyndactyly? (pages 179–180)

      S. S. Sidhu, Rekha Deshmukh and John M. Opitz

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310122

    3. Nondisjunction in down syndrome (pages 181–182)

      David B. Flannery and John M. Opitz

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310123

    4. Congenital diaphragmatic defects and maternal serum alphafetoprotein (pages 183–184)

      Jennifer A. Crossley, John L. Tolmie, David A. Aitken, Seonaig Easton, Giovanni Neri and John M. Opitz

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310124

  7. Rapid Publication Articles

    1. Top of page
    2. Masthead
    3. Brief Clinical Report
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Letter to the Editors
    8. Rapid Publication Articles
    9. Editorial Policy
    1. Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6 (pages 185–192)

      David A. Greenberg, Antonio V. Delgado-Escueta, Heidi Widelitz, Robert S. Sparkes, Lucy Treiman, Hector M. Maldonado, Min S. Park, Paul I. Terasaki, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310125

    2. 1987 ASHG workshop: Low maternal serum AFP screening for down syndrome (pages 193–196)

      Frank Greenberg, James F. Reynolds, James F. Reynolds and Frank Greenberg

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320310126

    3. AFP and age screening for down syndrome (pages 197–209)

      Professor Nicholas Wald, Howard Cuckle, John M. Opitz, James F. Reynolds and Frank Greenberg

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320310127

    4. California's experience with low MS-AFP results (pages 211–222)

      Linda Lustig, Susan Clarke, George Cunningham, Rhonda Schonberg, Gwynne Tompkinson, John M. Opitz, James F. Reynolds and Frank Greenberg

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310128

    5. The impact of MSAFP screening on genetic services, 1984–1986 (pages 223–230)

      Frank Greenberg, John M. Opitz, James F. Reynolds and Frank Greenberg

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320310129

    6. Maternal serum alpha-fetoprotein screening for down syndrome: Economic considerations (pages 231–245)

      J. Michael Swint, Frank Greenberg, John M. Opitz, James F. Reynolds and Frank Greenberg

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320310130

  8. Editorial Policy

    1. Top of page
    2. Masthead
    3. Brief Clinical Report
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Letter to the Editors
    8. Rapid Publication Articles
    9. Editorial Policy

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