116 related articles for article (PubMed ID: 9634368)
1. X-linked Wiskott-Aldrich syndrome in a girl.
Luzzatto L; Martini G
N Engl J Med; 1998 Jun; 338(25):1850-1. PubMed ID: 9634368
[No Abstract] [Full Text] [Related]
2. X-linked Wiskott-Aldrich syndrome in a girl.
Parolini O; Ressmann G; Haas OA; Pawlowsky J; Gadner H; Knapp W; Holter W
N Engl J Med; 1998 Jan; 338(5):291-5. PubMed ID: 9445409
[No Abstract] [Full Text] [Related]
3. Analysis of X-chromosome inactivation in bone marrow precursors from carriers of Wiskott-Aldrich syndrome and X-linked severe combined immunodeficiency: evidence that the Wiskott-Aldrich gene is expressed prior to granulocyte-macrophage colony-forming-unit.
Mantuano E; Candotti F; Giliani S; Parolini O; Lusardi M; Zucchi M; Lanfranchi A; Porta F; Airò P; Albertini A
Immunodeficiency; 1993; 4(1-4):271-6. PubMed ID: 8167717
[No Abstract] [Full Text] [Related]
4. X-linked Wiskott-Aldrich syndrome in a girl.
Cazzola M; Bergamaschi G
N Engl J Med; 1998 Jun; 338(25):1850; author reply 1851. PubMed ID: 9634367
[No Abstract] [Full Text] [Related]
5. X chromosome inactivation patterns in leucocyte populations of female carriers of Wiskott-Aldrich syndrome with an atypical presentation.
de Weers M; Mensink RG; Kraakman ME; Schuurman RK; Hendriks RW
Immunodeficiency; 1993; 4(1-4):267-9. PubMed ID: 8167716
[No Abstract] [Full Text] [Related]
6. X inactivation in females with X-linked disease.
Puck JM; Willard HF
N Engl J Med; 1998 Jan; 338(5):325-8. PubMed ID: 9445416
[No Abstract] [Full Text] [Related]
7. Molecular genetic analysis of X-linked immunodeficiencies.
Conley ME
Year Immunol; 1993; 7():162-7. PubMed ID: 8372504
[No Abstract] [Full Text] [Related]
8. Carrier detection in X-linked immunodeficiencies. II: An X inactivation assay based on differential methylation of a line-1 repeat at the DXS255 locus.
Hinds H; Craig IW; Chen ZY; Kraakman ME; Schuurman RK; Hendriks RW
Immunodeficiency; 1993; 4(1-4):213-5. PubMed ID: 8167703
[TBL] [Abstract][Full Text] [Related]
9. Carrier detection in X-linked immunodeficiencies. I: A PCR-based X chromosome inactivation assay at the MAOA locus.
Hendriks RW; Chen ZY; Hinds H; Schuurman RK; Craig IW
Immunodeficiency; 1993; 4(1-4):209-11. PubMed ID: 8167702
[TBL] [Abstract][Full Text] [Related]
10. Application of molecular analysis to genetic counseling in the Wiskott-Aldrich syndrome (WAS).
Notarangelo LD; Candotti F; Parolini O; Mantuano E; Giliani S; Lanfranchi A; Albertini A
DNA Cell Biol; 1993 Sep; 12(7):645-9. PubMed ID: 8397823
[TBL] [Abstract][Full Text] [Related]
11. The Wiskott-Aldrich syndrome.
Peacocke M; Siminovitch KA
Semin Dermatol; 1993 Sep; 12(3):247-54. PubMed ID: 8105860
[TBL] [Abstract][Full Text] [Related]
12. X-linked thrombocytopenia and Wiskott-Aldrich syndrome: similar regional assignment but distinct X-inactivation pattern in carriers.
De Saint-Basile G; Schlegel N; Caniglia M; Le Deist F; Kaplan C; Lecompte T; Piller F; Fischer A; Griscelli C
Ann Hematol; 1991 Aug; 63(2):107-10. PubMed ID: 1912030
[TBL] [Abstract][Full Text] [Related]
13. Cytogenetic studies in Wiskott-Aldrich syndrome: identification of a case with a 6p chromosome abnormality.
Johnson MP; Filipovich AH
Am J Med Genet; 1986 Mar; 23(3):765-73. PubMed ID: 3953675
[TBL] [Abstract][Full Text] [Related]
14. Mutations of the WASP gene in 10 Japanese patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
Itoh S; Nonoyama S; Morio T; Imai K; Okawa H; Ochs HD; Shimadzu M; Yata J
Int J Hematol; 2000 Jan; 71(1):79-83. PubMed ID: 10729999
[TBL] [Abstract][Full Text] [Related]
15. Multiple independent second-site mutations in two siblings with somatic mosaicism for Wiskott-Aldrich syndrome.
Boztug K; Germeshausen M; Avedillo Díez I; Gulacsy V; Diestelhorst J; Ballmaier M; Welte K; Maródi L; Chernyshova L; Klein C
Clin Genet; 2008 Jul; 74(1):68-74. PubMed ID: 18479478
[TBL] [Abstract][Full Text] [Related]
16. Immunodeficiency syndromes. X-linked agammaglobulinemia, common variable immunodeficiency, Chédiak-Higashi syndrome, Wiskott-Aldrich syndrome, and X-linked lymphoproliferative disorder.
Paller AS
Dermatol Clin; 1995 Jan; 13(1):65-71. PubMed ID: 7712652
[TBL] [Abstract][Full Text] [Related]
17. Immunodeficiency disease genes on the X chromosome.
Mensink EJ; Schuurman RK
Dis Markers; 1987 Sep; 5(3):129-40. PubMed ID: 3332256
[No Abstract] [Full Text] [Related]
18. A possible bichromatid mutation in a male gamete giving rise to a female mosaic for two different mutations in the X-linked gene WAS.
Dobbs AK; Yang T; Farmer DM; Howard V; Conley ME
Clin Genet; 2007 Feb; 71(2):171-6. PubMed ID: 17250667
[TBL] [Abstract][Full Text] [Related]
19. [Molecular genetic diagnosis of Wiskott-Aldrich syndrome].
Orth U; Rosenkranz W; Schwinger E; Holzgreve W; Gal A
Monatsschr Kinderheilkd; 1993 Sep; 141(9):728-31. PubMed ID: 8413349
[TBL] [Abstract][Full Text] [Related]
20. Presentation of Wiskott Aldrich syndrome as isolated thrombocytopenia.
Notarangelo LD; Parolini O; Faustini R; Porteri V; Albertini A; Ugazio AG
Blood; 1991 Mar; 77(5):1125-6. PubMed ID: 1995098
[No Abstract] [Full Text] [Related]
[Next] [New Search]