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Original Investigations
James C. Skare, Helen L. Grierson, John L. Sullivan, Robert L. Nussbaum, David T. Purtilo, Bakary S. Sylla, Gilbert M. Lenon, Dorothy S. Reilly, Bradley N. White and Aubrey Milunsky
Journal Article
Molecular genetic haplotype segregation studies in three families with X-linked lymphoproliferative disease
V. Schuster, S. Seidenspinner, T. Grimm, W. Kreß and S. Zielen, et al.
European Journal of Pediatrics, 1994, Volume 153, Number 6, Pages 432-437
Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on Xq
James C. Skare, John L. Sullivan and Aubrey Milunsky
Human Genetics, 1989, Volume 82, Number 4, Pages 349-353
Linkage studies in X-linked Alport's syndrome
S. Szpiro-Tapia, G. Bobrie, M. Guilloud-Bataille, S. Heuertz and C. Julier, et al.
Human Genetics, 1988, Volume 81, Number 1, Pages 85-87
Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosome
S. Szpiro-Tapia, A. Sefiani, M. Guilloud-Bataille, S. Heuertz and B. Marec, et al.
Human Genetics, 1988, Volume 81, Number 1, Pages 61-63
Interferon-gamma in a family with X-linked lymphoproliferative syndrome with acute Epstein-Barr virus infection
Motohiko Okano, Geoffrey M. Thiele, Roger H. Kobayashi, Jack R. Davis and Mark S. Synovec, et al.
Journal of Clinical Immunology, 1989, Volume 9, Number 1, Pages 48-54
A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome
N. T. Bech-Hansen, L. L. Field, A. M. Schramm, M. Reedyk and I. W. Craig, et al.
Human Genetics, 1989, Volume 84, Number 5, Pages 406-408
X-linked lymphoproliferative disease: Genetic lesions and clinical consequences
Andrew J. MacGinnitie and Raif Geha
Current Allergy and Asthma Reports, 2002, Volume 2, Number 5, Pages 361-367
Haplotype and multipoint linkage analysis in Finnish choroideremia families
Eeva-Marja Sankila, Thomas Lehner, Aldur W. Eriksson, Henrik Forsius and Jussi Kärnä, et al.
Human Genetics, 1989, Volume 84, Number 1, Pages 66-70
Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12
Steen Kølvraa, Torben A. Kruse, P. K. A. Jensen, Kirsten H. Linde and Søren R. Vestergaard, et al.
Human Genetics, 1986, Volume 74, Number 3, Pages 284-287
Book Chapter
Genetic Disorders of Immune Regulation
Carsten Speckmann, Jan Rohr and Stephan Ehl
2008, Primary Immunodeficiency Diseases, Pages 167-194
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