• Issue

    American Journal of Medical Genetics: Volume 78, Issue 1

    1-94
    16 June 1998
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Research Articles

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Some psychosocial aspects of nonlethal chondrodysplasias: I. Assessment using a life-styles questionnaire

Alasdair G.W. Hunter, 
  • Pages: 1-8
  • First Published: 06 December 1998
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Some psychosocial aspects of nonlethal chondrodysplasias: II. Depression and anxiety

Alasdair G.W. Hunter, 
  • Pages: 9-12
  • First Published: 06 December 1998
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Some psychosocial aspects of nonlethal chondrodysplasias: III. Self-esteem in children and adults

Alasdair G.W. Hunter, 
  • Pages: 13-16
  • First Published: 06 December 1998
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Some psychosocial aspects of nonlethal chondrodysplasias: IV. Dyadic scale of marital adjustment

Alasdair G.W. Hunter, 
  • Pages: 17-21
  • First Published: 06 December 1998
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Some psychosocial aspects of nonlethal chondrodysplasias: V. Assessment of personal social support using the personal resource questionnaire

Alasdair G.W. Hunter, 
  • Pages: 22-24
  • First Published: 06 December 1998
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Some psychosocial aspects of nonlethal chondrodysplasias: VI. Assessment of family interaction using the FACES II questionnaire

Alasdair G.W. Hunter, 
  • Pages: 25-29
  • First Published: 06 December 1998
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Functional health status of adults with achondroplasia

Nizar N. Mahomed,  Mark Spellmann,  Michael J. Goldberg, 
  • Pages: 30-35
  • First Published: 06 December 1998
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Clinical outcomes of four patients with microdeletion in the long arm of chromosome 2

Kenneth D. McMilin,  Jacob A. Reiss,  Michael G. Brown,  Mary H. Black,  Deborah A. Buckmaster,  Connie T. Durum,  Kristine A. Gunter,  Helen J. Lawce,  Toby L. Berry,  Olivia A. Lamb,  Cathy L. Olson,  Francoise F. Weeks,  Marvin J. Yoshitomi,  Peter B. Jacky,  Susan B. Olson,  R. Ellen Magenis, 
  • Pages: 36-43
  • First Published: 06 December 1998
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De novo apparently balanced complex chromosome rearrangement (CCR) involving chromosomes 4, 18, and 21 in a girl with mental retardation: Report and review

Jacqueline R. Batanian,  Marthand S. Eswara, 
  • Pages: 44-51
  • First Published: 06 December 1998
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4q33–qter deletion and absorptive hypercalciuria: Report of two unrelated girls

Keisaku Imamura,  Hidefumi Tonoki,  Keiko Wakui,  Yoshimitsu Fukushima,  Satoshi Sasaki,  Kazue Yausda,  Yasuo Takekoshi,  Hiroyuki Tochimaru, 
  • Pages: 52-54
  • First Published: 06 December 1998
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Interstitial dup(1p) with findings of Kabuki make-up syndrome

Ivan F.M. Lo,  Lauvena Y.K. Cheung,  Anita Y.Y. Ng,  Stephen T.S. Lam, 
  • Pages: 55-57
  • First Published: 06 December 1998
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Mutational analysis of the DTDST gene in a fetus with achondrogenesis type 1B

Guiming Cai,  Masahiro Nakayama,  Yuji Hiraki,  Keiichi Ozono, 
  • Pages: 58-60
  • First Published: 06 December 1998
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A rare form of spondylometaphyseal dysplasia-type A4

T. Duetting,  A. Schulze,  J. Troeger,  J. Spranger, 
  • Pages: 61-66
  • First Published: 06 December 1998
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Duplication of distal thumb phalanx in Shwachman-Diamond syndrome

Yigal Dror,  Peter Durie,  Peggy Marcon,  Melvin H. Freedman, 
  • Pages: 67-69
  • First Published: 06 December 1998
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New recessive syndrome characterized by increased chromosomal breakage and several findings which overlap with Fanconi anemia

Philip F. Giampietro,  Arleen D. Auerbach,  Ellen R. Elias,  Alyson Gutman,  Nancy J. Zellers,  Jessica G. Davis, 
  • Pages: 70-75
  • First Published: 06 December 1998
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Multiple schwannomas, multiple nevi, and multiple vaginal leiomyomas: A new dominant syndrome

Robert J. Gorlin,  Ioannis G. Koutlas, 
  • Pages: 76-81
  • First Published: 06 December 1998
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Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin

Yuan-Qing Wu,  V. Reid Sutton,  Elizabeth Nickerson,  James R. Lupski,  Lorraine Potocki,  Julie R. Korenberg,  Frank Greenberg,  Mayada Tassabehji,  Lisa G. Shaffer, 
  • Pages: 82-89
  • First Published: 06 December 1998

Miscellaneous

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Recent advances in molecular genetics of the Maghreb and the Middle East populations: The first Middle East Genetics Association of America (MEGA) conference

Dahmani M. Fathallah,  Koussay Dellagi,  Mazin B. Qumsiyeh,  Ahmad S. Teebi, 
  • Pages: 90-91
  • First Published: 06 December 1998

Letters to the Editor

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Gaucher type 2 disease: Identification of a novel transversion mutation in a French-Irish patient

Francis Y.M. Choy,  M. Lisa Humphries,  Yoav Ben-Yoseph, 
  • Pages: 92-93
  • First Published: 06 December 1998

Book Reviews

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A clinical guide to inherited metabolic diseases

Ahmad S. Teebi, 
  • Page: 94
  • First Published: 06 December 1998