1. Genetic basis of acanthosis nigricans in Mexican Americans and its association with phenotypes related to type 2 diabetes

   • James P. Burke
   • Ravindranath Duggirala
   • Michael P. Stern

   Original Investigation 20 April 2000 Pages: 467 - 472

2. Statistical and mutational analysis of chronic granulomatous disease in Japan with special reference to gp91-phox and p22-phox deficiency

   • Fuminari Ishibashi
   • Hiroyuki Nunoi
   • Shiro Kanegasaki

   Original Investigation 10 May 2000 Pages: 473 - 481

3. The mutation of Pro⁷⁸⁹ to Leu reduces the activity of the fast-twitch skeletal muscle sarco(endo)plasmic reticulum Ca²⁺ ATPase (SERCA1) and is associated with Brody disease

   • Alex Odermatt
   • Kimby Barton
   • David H. MacLennan

   Original Investigation 10 May 2000 Pages: 482 - 491

4. Splice-site mutation in TGM1 in congenital recessive ichthyosis in American families: molecular, genetic, genealogic, and clinical studies

   • Yuriy O. Shevchenko
   • John G. Compton
   • Sherri J. Bale

   Original Investigation 06 May 2000 Pages: 492 - 499

5. Interchromosomal effects for chromosome 21 in carriers of structural chromosome reorganizations determined by fluorescence in situ hybridization on sperm nuclei

   • Joan Blanco
   • Josep Egozcue
   • Francesca Vidal

   Original Investigation 19 April 2000 Pages: 500 - 505

6. Fine mapping of the constitutional translocation t(11;22)(q23;q11)

   • Isabel Tapia-Páez
   • Kevin P. O'Brien
   • Jan P. Dumanski

   Original Investigation 20 April 2000 Pages: 506 - 516

7. Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies

   • Anna M. Estop
   • Kathy Cieply
   • Eleanor Feingold

   Original Investigation 18 April 2000 Pages: 517 - 524

8. Variation in alphoid DNA size and trisomy 21: a possible cause of nondisjunction

   • Klio Maratou
   • Yasmeen Siddique
   • Gail E. Davies

   Original Investigation 11 April 2000 Pages: 525 - 530

9. A 5-base insertion in the γC-crystallin gene is associated with autosomal dominant variable zonular pulverulent cataract

   • Zhaoxia Ren
   • Anren Li
   • J. Fielding Hejtmancik

   Original Investigation 14 April 2000 Pages: 531 - 537

10. Multi-allelic origin of congenital disorder of glycosylation (CDG)-Ic

    • Timo Imbach
    • Stephanie Grünewald
    • Thierry Hennet

    Original Investigation 19 April 2000 Pages: 538 - 545

11. Association of the low-density lipoprotein receptor gene with obesity in Native American populations

    • Vanessa S. Mattevi
    • Carlos E. A. Coimbra Jr
    • Mara H. Hutz

    Original Investigation 10 May 2000 Pages: 546 - 552

12. A genetic study of Hodgkin's lymphoma: an estimate of heritability and anticipation based on the familial cancer database in Sweden

    • Yin Yao Shugart
    • Kari Hemminki
    • Chuanhui Dong

    Original Investigation 13 April 2000 Pages: 553 - 556

13. Autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly) is linked to chromosome 22q12-13

    • Michael J. Kelley
    • William Jawien
    • Jeannette F. Korczak

    Original Investigation 14 April 2000 Pages: 557 - 564

14. Analysis of genetic polymorphisms in the transforming growth factor-β1 gene and the risk of Alzheimer's disease

    • Erin K. Luedecking
    • Steven T. DeKosky
    • M. Ilyas Kamboh

    Original Investigation 10 May 2000 Pages: 565 - 569

15. Erratum to Mutation and polymorphism analysis of the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor in congenital insensitivity to pain with anhidrosis (CIPA) families

    • Yuichi Miura
    • Sek Mardy
    • Yasuhiro Indo

    Erratum 03 May 2000 Pages: 575 - 575