Pescia G - Search Results

1

[Molecular analysis of 68 Swiss-Romance subjects at risk for fragile X syndrome].

Schorderet DF, Thonney F, Pillet N, Delozier-Blanchet C, Marguerat P, Pescia G. Schorderet DF, et al. Among authors: pescia g. Rev Med Suisse Romande. 1993 Apr;113(4):309-11. Rev Med Suisse Romande. 1993. PMID: 8502886 French. No abstract available.

2

[Towards systematic screening for mucoviscidosis?].

Pescia G, Van Melle G, Thonney F, Auer C, Schorderet D, Fokstuen S. Pescia G, et al. Rev Med Suisse Romande. 1993 Apr;113(4):281-6. Rev Med Suisse Romande. 1993. PMID: 7684853 French. No abstract available.

3

[The Vaud register of congenital abnormalities].

Addor MC, Pescia G, Marguerat P. Addor MC, et al. Among authors: pescia g. Rev Med Suisse Romande. 1993 Apr;113(4):265-71. Rev Med Suisse Romande. 1993. PMID: 8502882 French. No abstract available.

4

[Fluorescent in-situ hybridization and molecular cytogenetics].

Thonney F, Pescia G. Thonney F, et al. Among authors: pescia g. Rev Med Suisse Romande. 1993 Apr;113(4):305-8. Rev Med Suisse Romande. 1993. PMID: 8502885 French. No abstract available.

5

[The genetics of mucoviscidosis 50 years later].

Pescia G, Marguerat P. Pescia G, et al. Rev Med Suisse Romande. 1987 Jul;107(7):577-80. Rev Med Suisse Romande. 1987. PMID: 3629070 French. No abstract available.

6

[Defects in neural tube closure in the Vaud canton 1980-1992. The impact of prenatal diagnosis].

Marguerat P, Addor MC, Pescia G, Maillard-Brignon C, Laurini RN, Hohlfeld P, Vial Y, Weihs D. Marguerat P, et al. Among authors: pescia g. Rev Med Suisse Romande. 1994 Oct;114(10):851-9. Rev Med Suisse Romande. 1994. PMID: 7526434 French. No abstract available.

7

[Alpha-fetoprotein and chromosome aberrations: what else? Results of a prospective study concerning 15,533 pregnancies].

Marguerat P, Weihs D, Pescia G, Gaide AC, Addor MC, Nguyen The H. Marguerat P, et al. Among authors: pescia g. Rev Med Suisse Romande. 1993 Apr;113(4):273-6. Rev Med Suisse Romande. 1993. PMID: 7684851 French. No abstract available.

8

[Triple screening for trisomy 21: prospective results of 7039 assessments].

Pescia G, Dao MH, Weihs D, Gaide AC, Loertscher A, Hohlfeld P, Marguerat P, Nguyen The H, Paccaud F, Maillard C, et al. Pescia G, et al. Rev Med Suisse Romande. 1993 Apr;113(4):277-80. Rev Med Suisse Romande. 1993. PMID: 7684852 French. No abstract available.

9

[Prenatal diagnosis of genetic diseases: Lausanne experience 1989-1993].

Fokstuen S, Pescia G, Addor MC, Gaide AC, Marguerat P, Maillard C, Vial Y, Hohlfeld P, Nguyen The H. Fokstuen S, et al. Among authors: pescia g. Rev Med Suisse Romande. 1994 Dec;114(12):1055-65. Rev Med Suisse Romande. 1994. PMID: 7817068 Review. French. No abstract available.

10

An additional family with Startle disease and a G1192A mutation at the alpha 1 subunit of the inhibitory glycine receptor gene.

Schorderet DF, Pescia G, Bernasconi A, Regli F. Schorderet DF, et al. Among authors: pescia g. Hum Mol Genet. 1994 Jul;3(7):1201. doi: 10.1093/hmg/3.7.1201. Hum Mol Genet. 1994. PMID: 7981700 No abstract available.

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