Griscelli C - Search Results

1

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: griscelli c. Am J Hum Genet. 1990 May;46(5):906-11. Am J Hum Genet. 1990. PMID: 1971143 Free PMC article.

2

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. Among authors: griscelli c. Hum Genet. 1992 May;89(2):223-8. doi: 10.1007/BF00217127. Hum Genet. 1992. PMID: 1350264 Clinical Trial.

3

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. De Saint-Basile G, et al. Among authors: griscelli c. Ann Hematol. 1991 Aug;63(2):107-10. doi: 10.1007/BF01707282. Ann Hematol. 1991. PMID: 1912030

4

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: griscelli c. Hum Genet. 1987 Oct;77(2):172-4. doi: 10.1007/BF00272387. Hum Genet. 1987. PMID: 2888720

5

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. Among authors: griscelli c. Hum Genet. 1988 Sep;80(1):85-9. doi: 10.1007/BF00451463. Hum Genet. 1988. PMID: 3417309

6

Fine mapping of the human SCIDX1 locus at Xq12-13.1.

Markiewicz S, DiSanto JP, Chelly J, Fairweather N, Le Marec B, Griscelli C, Graeber MB, Müller U, Fischer A, Monaco AP, et al. Markiewicz S, et al. Among authors: griscelli c. Hum Mol Genet. 1993 Jun;2(6):651-4. doi: 10.1093/hmg/2.6.651. Hum Mol Genet. 1993. PMID: 8353486

7

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. Among authors: griscelli c. J Clin Invest. 1992 Mar;89(3):861-6. doi: 10.1172/JCI115665. J Clin Invest. 1992. PMID: 1347296 Free PMC article.

8

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: griscelli c. Am J Med Genet. 1992 Jul 15;43(5):885-7. doi: 10.1002/ajmg.1320430527. Am J Med Genet. 1992. PMID: 1642281

9

Two complementation groups account for most cases of inherited MHC class II deficiency.

Lisowska-Grospierre B, Fondaneche MC, Rols MP, Griscelli C, Fischer A. Lisowska-Grospierre B, et al. Among authors: griscelli c. Hum Mol Genet. 1994 Jun;3(6):953-8. doi: 10.1093/hmg/3.6.953. Hum Mol Genet. 1994. PMID: 7951244

10

Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene.

Pastural E, Barrat FJ, Dufourcq-Lagelouse R, Certain S, Sanal O, Jabado N, Seger R, Griscelli C, Fischer A, de Saint Basile G. Pastural E, et al. Among authors: griscelli c. Nat Genet. 1997 Jul;16(3):289-92. doi: 10.1038/ng0797-289. Nat Genet. 1997. PMID: 9207796

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