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Cooking Up Fun! A Youth Development Strategy that Promotes Independent Food Skills

Journal of nutrition education and behavior, 2006-09, Vol.38 (5), p.321-323

2006

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G.P.5.08 Myofibrillar myopathies: The Lausanne experience with DES mutations in 11 patients

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.570-570

2009

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Evidence of Somatic and Germinal Mosaicism in Pseudo–Low-Penetrant Hereditary Retinoblastoma, by Constitutional and Single-Sperm Mutation Analysis

American journal of human genetics, 1998-12, Vol.63 (6), p.1903-1907

1998

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Further delineation of the facial 13q14 deletion syndrome in 13 retinoblastoma patients

Ophthalmic genetics, 2001, Vol.22 (1), p.11-18

2001

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Molecular characterization of the deletion in retinoblastoma patients with 13q14 cytogenetic anomalies

Ophthalmic genetics, 2001, Vol.22 (1), p.1-10

2001

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Fetus with two identical reciprocal translocations: Description of a rare complication of consanguinity

American journal of medical genetics. Part A, 2006-04, Vol.140A (7), p.769-774

2006

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Prognostic factors associated with loss of heterozygosity at the RB1 locus in retinoblastoma

Ophthalmic genetics, 1997, Vol.18 (1), p.7-12

1997

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Constitutional Karyotype in Retinoblastoma Case Report and Review of Literature

Ophthalmic genetics, 1989, Vol.10 (2), p.129-149

1989

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Chromosome analysis of chorionic villi: technique and results

Contributions to gynecology and obstetrics, 1986, Vol.15, p.70

1986

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A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotype

Human genetics, 1997-08, Vol.100 (2), p.220-223

1997

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Fluorescent in-situ hybridization and molecular cytogenetics

Revue medicale de la Suisse romande, 1993-04, Vol.113 (4), p.305

1993

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Applications de l'hybridation in situ fluorescente (FISH) dans le diagnostic prénatal

Archives of gynecology and obstetrics, 1994-12, Vol.255 (S2), p.S367-S371

1994

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Quick prenatal diagnosis using FISH in the analysis of non-cultured amniotic fluid cells

Revue medicale de la Suisse romande, 2000-05, Vol.120 (5), p.401

2000

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Applications of fluorescence in situ hybridization in prenatal diagnosis

Archives of gynecology and obstetrics, 1994, Vol.255 Suppl 2, p.S367-S371

1994

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Paternal selection favoring mutant alleles of the retinoblastoma susceptibility gene

Human genetics, 1992-07, Vol.89 (5), p.508-512

1992

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Residues of agricultural chemicals on fruits and vegetables: pesticide use and regulatory issues

Nutrition today (Annapolis), 1989-11, Vol.24 (6), p.6-12

1989

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Fluorescent in situ hybridization (FISH). Diagnostic aide in certain chromosomal anomalies

Revue medicale de la Suisse romande, 2000-05, Vol.120 (5), p.389

2000

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Clinical applications of molecular diagnosis of retinoblastoma ain 15 families

Klinische Monatsblätter für Augenheilkunde, 1995-05, Vol.206 (5), p.336

1995

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Sex mutation ratio in retinoblastoma and retinoma: relevance to genetic counseling

Klinische Monatsblätter für Augenheilkunde, 1996-05, Vol.208 (5), p.400

1996

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Retinoblastoma: clinical and molecular diagnostic aspects

Praxis (Bern. 1994), 1996-08, Vol.85 (35), p.1058

1996

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Association between haplotypes and specific mutations in Swiss cystic fibrosis families

Pediatric research, 1991-10, Vol.30 (4), p.304-308

1991

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Cytogenetic analysis of 570 first trimester chorionic villi samplings: technique and results

Annales de génétique, 1988, Vol.31 (1), p.14

1988

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

Revue medicale de la Suisse romande, 1993-04, Vol.113 (4), p.309

1993

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Towards systematic screening for mucoviscidosis?

Revue medicale de la Suisse romande, 1993-04, Vol.113 (4), p.281

1993

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Evaluation of a supermarket nutrition education program

Journal of nutrition education, 1982-01, Vol.14 (4), p.141-145

1982

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Cooking Up Fun! A Youth Development Strategy that Promotes Independent Food Skills

G.P.5.08 Myofibrillar myopathies: The Lausanne experience with DES mutations in 11 patients

Evidence of Somatic and Germinal Mosaicism in Pseudo–Low-Penetrant Hereditary Retinoblastoma, by Constitutional and Single-Sperm Mutation Analysis

Further delineation of the facial 13q14 deletion syndrome in 13 retinoblastoma patients

Molecular characterization of the deletion in retinoblastoma patients with 13q14 cytogenetic anomalies

Fetus with two identical reciprocal translocations: Description of a rare complication of consanguinity

Prognostic factors associated with loss of heterozygosity at the RB1 locus in retinoblastoma

Constitutional Karyotype in Retinoblastoma Case Report and Review of Literature

Chromosome analysis of chorionic villi: technique and results

A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotype

Fluorescent in-situ hybridization and molecular cytogenetics

Applications de l'hybridation in situ fluorescente (FISH) dans le diagnostic prénatal

Quick prenatal diagnosis using FISH in the analysis of non-cultured amniotic fluid cells

Applications of fluorescence in situ hybridization in prenatal diagnosis

Paternal selection favoring mutant alleles of the retinoblastoma susceptibility gene

Residues of agricultural chemicals on fruits and vegetables: pesticide use and regulatory issues

Fluorescent in situ hybridization (FISH). Diagnostic aide in certain chromosomal anomalies

Clinical applications of molecular diagnosis of retinoblastoma ain 15 families

Sex mutation ratio in retinoblastoma and retinoma: relevance to genetic counseling

Retinoblastoma: clinical and molecular diagnostic aspects

Association between haplotypes and specific mutations in Swiss cystic fibrosis families

Cytogenetic analysis of 570 first trimester chorionic villi samplings: technique and results

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

Towards systematic screening for mucoviscidosis?

Evaluation of a supermarket nutrition education program

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