• Issue

    American Journal of Medical Genetics: Volume 93, Issue 1

    1-79
    3 July 2000
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Yellow nail syndrome presenting as non-immune hydrops: Second case report

Jennie Slee,  John Nelson,  Jan Dickinson,  Peter Kendall,  Anne Halbert, 
  • Pages: 1-4
  • First Published: 12 June 2000
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New form of idiopathic osteolysis: Nodulosis, arthropathy and osteolysis (NAO) syndrome

Sulaiman M. Al-Mayouf,  Mahmoud Majeed,  Claes Hugosson,  Sultan Bahabri, 
  • Pages: 5-10
  • First Published: 12 June 2000
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Inherited multicentric osteolysis with arthritis: A variant resembling Torg syndrome in a Saudi family

Aida Al Aqeel,  Wafa Al Sewairi,  Burhan Edress,  Robert J. Gorlin,  Robert J. Desnick,  John A. Martignetti, 
  • Pages: 11-18
  • First Published: 12 June 2000

Brief Clinical Report

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Distal limb deficiencies, oral involvement, and renal defect: Report of a third patient and confirmation of a distinct entity

K. Keymolen,  R. Van Damme-Lombaerts,  A. Verloes,  J.P. Fryns, 
  • Pages: 19-21
  • First Published: 12 June 2000
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Clinical findings in a patient with FGFR1 P252R mutation and comparison with the literature

T. Roscioli,  S. Flanagan,  P. Kumar,  J. Masel,  M. Gattas,  V.J. Hyland,  I.A. Glass, 
  • Pages: 22-28
  • First Published: 12 June 2000
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Genetic testing, adverse selection, and the demand for life insurance

Cathleen D. Zick,  Ken R. Smith,  Robert N. Mayer,  Jeffery R. Botkin, 
  • Pages: 29-39
  • First Published: 12 June 2000
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Multicolor fluorescence in situ hybridization analysis of meiotic chromosome segregation in a 47,XYY male and a review of the literature

Qinghua Shi,  Renee H. Martin, 
  • Pages: 40-46
  • First Published: 12 June 2000
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Syndrome of short stature, mental deficiency, microcephaly, ectodermal dysplasia, and multiple skeletal anomalies

Miroslav Dumić,  Marijana Cvitanovic,  Jasenka Ille,  Kristina Potocki, 
  • Pages: 47-51
  • First Published: 12 June 2000
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Severe phenotypes associated with inactive ring X chromosomes

Barbara R. Migeon,  Margareet Ausems,  Jacques Giltay,  Camille Hasley-Royster,  Ethan Kazi,  Thomas J. Lydon,  John J.M. Engelen,  Gerald V. Raymond, 
  • Pages: 52-57
  • First Published: 12 June 2000
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Are hereditary hemochromatosis mutations involved in Alzheimer disease?

Sharon Moalem,  Maire E. Percy,  David F. Andrews,  Theo P.A. Kruck,  Simon Wong,  Arthur J. Dalton,  Pankaj Mehta,  Bettye Fedor,  Andrew C. Warren, 
  • Pages: 58-66
  • First Published: 12 June 2000
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Severe acro-renal-uterine-mandibular syndrome

Jane A. Evans,  Susan Phillips,  Martin Reed,  Bernard N. Chodirker, 
  • Pages: 67-73
  • First Published: 12 June 2000

Letter to the Editor

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Tetracuspid aortic valve in a patient with 22q11.2 microdeletion

Masao Nakagawa,  Nobuhiko Okamoto,  Hidetoshi Fujino,  Noriko Watanabe,  Masahiko Okuno, 
  • Pages: 74-75
  • First Published: 12 June 2000
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Trisomy of 5p and marker chromosomes

U.G. Froster,  H. Reichenbach, 
  • Page: 76
  • First Published: 12 June 2000
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Hemochromatosis gene nomenclature

H.M. Wain,  J.A. White,  E. Bruford,  S. Povey, 
  • Page: 77
  • First Published: 12 June 2000

Book Review

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Genetic diseases of the eye, edited by Elias I Traboulsi

Mohnish Suri, 
  • Pages: 78-79
  • First Published: 12 June 2000