Zobrazeno 1 - 10 of 80 pro vyhledávání: '"F, Thonney"'
2
[Quick prenatal diagnosis using FISH in the analysis of non-cultured amniotic fluid cells]
Autor: P, Marguerat, A C, Gaide, F, Thonney, D, Schorderet
Publikováno v: Revue medicale de la Suisse romande. 120(5)
We report our experience with fluorescence in situ hybridization (FISH) on uncultured amniocytes and standard cytogenetic analysis. The method have been suggested to 259 patients and performed for 199 amniotic fluid samples. Commercially available ch
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cbbf63d7d5dec39746895dc22799cbd3
https://pubmed.ncbi.nlm.nih.gov/10911743
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4
[Assisted fertilization in azoospermic men: results of CHUV from 1994 to 1997]
Autor: M, Wisard, A, Senn, F, Thonney, D F, Schorderet, M, Germond
Publikováno v: Schweizerische medizinische Wochenschrift. 129(11)
In vitro fertilisation (IVF) and intracytoplasmic sperm injection (ICSI) have revolutionised the treatment and prognosis of oligo-terato-asthenozoospermia (OTA). Sperm extraction in the vas deferens, the epididymis (MESA: with epididymal sperm aspira
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9de3122e796c654a5df6b54f5c021b08
https://pubmed.ncbi.nlm.nih.gov/10226323
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5
Prognostic factors associated with loss of heterozygosity at the RB1 locus in retinoblastoma
Autor: Aubin Balmer, E. Héon, G. Pescia, F. Thonney, Sylvie Uffer, G. van Melle, H. P. Rutz, Francis L. Munier, Daniel F. Schorderet
Publikováno v: Ophthalmic genetics. 18(1)
The nature of the tumorigenic mutation was analyzed in 30 retinoblastoma (Rb) tumors (16 non-hereditary and 14 hereditary) and categorized into loss of heterozygosity (LOH) or retention of heterozygosity (non-LOH) at the RB1 locus. These genotypic ch
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c16d3604619ced569ebb51830259e61
https://pubmed.ncbi.nlm.nih.gov/9134545
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6
[Retinoblastoma: clinical and molecular diagnostic aspects]
Autor: F, Thonney, F L, Munier, A, Balmer, G, Pescia, D F, Schorderet
Publikováno v: Praxis. 85(35)
Retinoblastoma, a tumor of the immature retina concerns babies and young infants in particular. They make up for 14% of malignomas in the first years of life. There are two types of retinoblastoma: In the first two alleles of the gene Rb1 must be ina
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9ca3c19ca7c10884e21d153b9f1414a3
https://pubmed.ncbi.nlm.nih.gov/8848678
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7
[Clinical applications of molecular diagnosis of retinoblastoma ain 15 families]
Autor: B, Lendi, G, Pescia, F, Thonney, A, Balmer, F, Munier
Publikováno v: Klinische Monatsblatter fur Augenheilkunde. 206(5)
In 40% retinoblastoma (Rb) results from a hereditary mutation of the Rb susceptibility gene (RB1). In this study, we tested the usefulness of intragenic DNA analysis for ophthalmologic follow-up in affected families.Molecular analysis was performed o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::24c06c13f46b7bd4ee9170a304965264
https://pubmed.ncbi.nlm.nih.gov/7609380
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