de Saint Basile G - Search Results

1

Ménasché G, Fischer A, de Saint Basile G. Ménasché G, et al. Among authors: de saint basile g. Am J Hum Genet. 2002 Nov;71(5):1237-8; author reply 1238. doi: 10.1086/344140. Am J Hum Genet. 2002. PMID: 12452176 Free PMC article. No abstract available.

2

Genetic study of a new X-linked recessive immunodeficiency syndrome.

de Saint-Basile G, Le Deist F, Caniglia M, Lebranchu Y, Griscelli C, Fischer A. de Saint-Basile G, et al. J Clin Invest. 1992 Mar;89(3):861-6. doi: 10.1172/JCI115665. J Clin Invest. 1992. PMID: 1347296 Free PMC article.

3

Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 beta.

de Saint Basile G, Notarangelo LD, Bonaiti-Pellié C, Doussau M, Prolini O, Craig IW, Ugazio A, Griscelli C, Fischer A. de Saint Basile G, et al. Hum Genet. 1992 May;89(2):223-8. doi: 10.1007/BF00217127. Hum Genet. 1992. PMID: 1350264 Clinical Trial.

4

Carrier detection and prenatal diagnosis of X-linked agammaglobulinemia.

Journet O, Durandy A, Doussau M, Le Deist F, Couvreur J, Griscelli C, Fischer A, de Saint-Basile G. Journet O, et al. Among authors: de saint basile g. Am J Med Genet. 1992 Jul 15;43(5):885-7. doi: 10.1002/ajmg.1320430527. Am J Med Genet. 1992. PMID: 1642281

5

X-linked immunodeficiencies: clues to genes involved in T- and B-cell differentiation.

de Saint Basile G, Fischer A. de Saint Basile G, et al. Immunol Today. 1991 Dec;12(12):456-61. doi: 10.1016/0167-5699(91)90019-p. Immunol Today. 1991. PMID: 1686172 Review.

6

Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndrome.

Arveiler B, de Saint-Basile G, Fischer A, Griscelli C, Mandel JL. Arveiler B, et al. Among authors: de saint basile g. Am J Hum Genet. 1990 May;46(5):906-11. Am J Hum Genet. 1990. PMID: 1971143 Free PMC article.

7

Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome).

de Saint-Basile G, Le Deist F, de Villartay JP, Cerf-Bensussan N, Journet O, Brousse N, Griscelli C, Fischer A. de Saint-Basile G, et al. Among authors: de villartay jp. J Clin Invest. 1991 Apr;87(4):1352-9. doi: 10.1172/JCI115139. J Clin Invest. 1991. PMID: 2010548 Free PMC article.

8

Close linkage of hypervariable marker DXS255 to disease locus of Wiskott-Aldrich syndrome.

de Saint Basile G, Arveiler B, Fraser NJ, Boyd Y, Graig IW, Griscelli G, Fischer A. de Saint Basile G, et al. Lancet. 1989 Dec 2;2(8675):1319-21. doi: 10.1016/s0140-6736(89)91920-x. Lancet. 1989. PMID: 2574264

9

Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA).

Malcolm S, de Saint Basile G, Arveiler B, Lau YL, Szabo P, Fischer A, Griscelli C, Debre M, Mandel JL, Callard RE, et al. Malcolm S, et al. Among authors: de saint basile g. Hum Genet. 1987 Oct;77(2):172-4. doi: 10.1007/BF00272387. Hum Genet. 1987. PMID: 2888720

10

Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotype.

de Saint-Basile G, Bohler MC, Fischer A, Cartron J, Dufier JL, Griscelli C, Orkin SH. de Saint-Basile G, et al. Hum Genet. 1988 Sep;80(1):85-9. doi: 10.1007/BF00451463. Hum Genet. 1988. PMID: 3417309

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