65 related articles for article (PubMed ID: 8516674)
1. David's victory. Gene causing "bubble boy" illness is finally found.
Rennie J
Sci Am; 1993 Jun; 268(6):34-5. PubMed ID: 8516674
[No Abstract] [Full Text] [Related]
2. Physical and genetic mapping in the region of Xq12-21, which contains the locus for X-linked severe combined immunodeficiency.
Jones A; Morris T; de Alwis M; Malcolm S; Levinsky RJ; Kinnon C
Immunodeficiency; 1993; 4(1-4):259-62. PubMed ID: 8167714
[No Abstract] [Full Text] [Related]
3. [X-linked severe combined immunodeficiency].
Kumaki S
Nihon Rinsho Meneki Gakkai Kaishi; 2002 Feb; 25(1):140-5. PubMed ID: 11963175
[No Abstract] [Full Text] [Related]
4. Genetic basis of the primary immunodeficiency syndromes.
Adelman DC
West J Med; 1995 Oct; 163(4):373-4. PubMed ID: 7483602
[No Abstract] [Full Text] [Related]
5. X-linked SCID and other defects of cytokine pathways.
Uribe L; Weinberg KI
Semin Hematol; 1998 Oct; 35(4):299-309. PubMed ID: 9801259
[TBL] [Abstract][Full Text] [Related]
6. European Society of Human Genetics. Abstracts from symposium on "X-linked diseases". Madrid, Spain, September 29-October 2, 1982.
Clin Genet; 1983 Mar; 23(3):195-259. PubMed ID: 6682728
[No Abstract] [Full Text] [Related]
7. The molecular basis of X-linked agammaglobulinemia, hyper-IgM syndrome, and severe combined immunodeficiency in humans.
Aruffo A; Hollenbaugh D; Wu LH; Ochs HD
Curr Opin Hematol; 1994 Jan; 1(1):12-8. PubMed ID: 9371254
[TBL] [Abstract][Full Text] [Related]
8. Lyon hypothesis--a look back.
Shankar R
Indian J Pathol Microbiol; 1990 Jan; 33(1):112-4. PubMed ID: 2394470
[No Abstract] [Full Text] [Related]
9. Clinical research. Gene therapy a suspect in leukemia-like disease.
Marshall E
Science; 2002 Oct; 298(5591):34-5. PubMed ID: 12364755
[No Abstract] [Full Text] [Related]
10. [Genetic basis for Rett disease].
Midro AT; Panasiuk B
Postepy Hig Med Dosw; 1997; 51(4):399-419. PubMed ID: 9446102
[TBL] [Abstract][Full Text] [Related]
11. Gene therapy of severe combined immunodeficiencies.
Cavazzana-Calvo M; Hacein-Bey S; Yates F; de Villartay JP; Le Deist F; Fischer A
J Gene Med; 2001; 3(3):201-6. PubMed ID: 11437325
[TBL] [Abstract][Full Text] [Related]
12. Efficient detection of thirty-seven new IL2RG mutations in human X-linked severe combined immunodeficiency.
Niemela JE; Puck JM; Fischer RE; Fleisher TA; Hsu AP
Clin Immunol; 2000 Apr; 95(1 Pt 1):33-8. PubMed ID: 10794430
[TBL] [Abstract][Full Text] [Related]
13. [X-linked mental retardation syndromes].
Kurosawa K
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):123-30. PubMed ID: 11057166
[No Abstract] [Full Text] [Related]
14. Sib understanding of genetics and attitudes toward carrier testing for X-linked severe combined immunodeficiency.
Fanos JH; Davis J; Puck JM
Am J Med Genet; 2001 Jan; 98(1):46-56. PubMed ID: 11426455
[TBL] [Abstract][Full Text] [Related]
15. Genetic mosaicism: what Gregor Mendel didn't know.
Hirschhorn R
J Clin Invest; 1995 Feb; 95(2):443-4. PubMed ID: 7860724
[No Abstract] [Full Text] [Related]
16. Intrinsic defects of B cell function in X-linked severe combined immunodeficiency.
White H; Thrasher A; Veys P; Kinnon C; Gaspar HB
Eur J Immunol; 2000 Mar; 30(3):732-7. PubMed ID: 10741387
[TBL] [Abstract][Full Text] [Related]
17. Analysing human developmental abnormalities.
Winter RM
Bioessays; 1996 Dec; 18(12):965-71. PubMed ID: 8976153
[TBL] [Abstract][Full Text] [Related]
18. Intriguing association between disease associated unstable trinucleotide repeat and CpG island.
Gourdon G; Dessen P; Lia AS; Junien C; Hofmann-Radvanyi H
Ann Genet; 1997; 40(2):73-7. PubMed ID: 9259953
[TBL] [Abstract][Full Text] [Related]
19. Temporary halt on gene therapy trials.
FDA Consum; 2003; 37(2):6. PubMed ID: 12715756
[No Abstract] [Full Text] [Related]
20. Common X-linked disorders.
Phillips JA
J Tenn Med Assoc; 1986 Jul; 79(7):435-6. PubMed ID: 3747507
[No Abstract] [Full Text] [Related]
[Next] [New Search]