Marie Louise Briard: search on Z-Library

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1

Anomalies chromosomiques

Briard, Marie-Louise, Morichon-Delvallez, Nicole

Journal:

EMC - Traité de Médecine AKOS

Year:

2006

Language:

french

File:

PDF, 143 KB

french, 2006

2

Linkage disequilibrium between phenylketonuria and RFLP haplotype 1 at the phenylalanine hydroxylase locus in Portugal

Catherine Caillaud, Laura Vilarinho, Antoine Vilarinho, Françoise Rev, Monique Bertheion, Rosario Santos, Stanislas Lyonnet, Marie-Louise Briard, Rui Osorio, Jean Rev, Arnold Munnich

Journal:

Year:

1992

Language:

english

File:

PDF, 578 KB

english, 1992

3

BBBG syndrome or opitz syndrome: New family

Alain Verloes, Martine Le Merrer, Marie-Louise Briard

Journal:

American Journal of Medical Genetics Part A

Year:

1989

Language:

english

File:

PDF, 409 KB

english, 1989

4

Neonatal myasthenia gravis: Anti-acetylcholine receptor antibodies in the amniotic fluid

Evelyne Morel, Jean-François Bach, Marie-Louise Briard, Jean-Pierre Aubry

Journal:

Journal of Neuroimmunology

Year:

1984

Language:

english

File:

PDF, 203 KB

english, 1984

5

Embryonic testicular regression syndrome: Variable phenotypic expression in siblings

Nathalie Josso, Marie-Louise Briard

Journal:

The Journal of Pediatrics

Year:

1980

Language:

english

File:

PDF, 1.92 MB

english, 1980

6

A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1

Kaplan, Josseline, Gerber, Sylvie, Larget-Piet, Dominique, Rozet, Jean-Michel, Dollfus, Hélène, Dufier, Jean-Louis, Odent, Sylvie, Postel-Vinay, Anne, Janin, Nicolas, Briard, Marie-Louise

Journal:

Nature Genetics

Year:

1993

File:

PDF, 477 KB

1993

7

Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31–p22.13 region

A. Toutain, Nathalie Ronce, Benoît Dessay, Laura Robb, Christine Francannet, Martine Le Merrer, Marie-Louise Briard, Josseline Kaplan, Claude Moraine

Journal:

Year:

1997

Language:

english

File:

PDF, 76 KB

english, 1997

8

Sister chromatid exchanges in patients with retinoblastoma

Hera Der-Sarkissian, Catherine Bonaïti-Pellié, Marie-Louise Briard-Guillemot, Jean-Michel Zucker

Journal:

Cancer Genetics and Cytogenetics

Year:

1982

Language:

english

File:

PDF, 433 KB

english, 1982

9

Parental age in retinoblastoma

Catherine Pellié, Marie-Louise Briard, Josué Feingold, Jean Frézal

Journal:

Year:

1973

Language:

english

File:

PDF, 268 KB

english, 1973

10

A gene for Leber's congenital amaurosis maps to chromosome 17p

Camuzat, Agnès, Dollfus, Hélène, Rozet, Jean-Michel, Gerber, Sylvie, Bonneau, Dominique, Bonnemaison, Michèle, Briard, Marie-Louise, Dufier, Jean-Louis, Ghazi, Imad, Leowski, Corinne, Weissenbach, Jea

Journal:

Human Molecular Genetics

Year:

1995

Language:

english

File:

PDF, 519 KB

english, 1995

11

Ethical aspects of neonatal screening for sickle cell disease in Western European countries

Mariane De Montalembert, Doris Bonnet, Danielle Lena-Russo, Marie Louise Briard

Journal:

Acta Paediatrica

Year:

2005

Language:

english

File:

PDF, 55 KB

english, 2005

12

The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52

Lyonnet, Stanislas, Pelet, Anna, Royer, Ghislaine, Delrieu, Olivier, Serville, Françoise, Le Marec, Bernard, Gruensteudel, Anita, Pfeiffer, Rudolf A., Briard, Marie-Louise, Dubay, Christopher

Journal:

Year:

1992

Language:

english

File:

PDF, 269 KB

english, 1992

13

Consanguinity in Multifactorial Inheritance

Bona&iuml, ti, Catherine, Demenais, Florence, Briard, Marie-Louise, Feingold, Josu&eacute,

Journal:

Year:

1978

Language:

english

File:

PDF, 1.02 MB

english, 1978

14

Congenital glaucoma: Genetic models

Florence Demenais, Catherine Bonaïti, Marie-Louise Briard, Josué Feingold, Jean Frézal

Journal:

Year:

1979

Language:

english

File:

PDF, 683 KB

english, 1979

15

Segregation analysis in hereditary retinoblastoma

Catherine Bonaïti-Pellié, Marie Louise Briard-Guillemot

Journal:

Year:

1981

Language:

english

File:

PDF, 583 KB

english, 1981

16

Spectrum of phenylketonuria mutations in Western Europe and North Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus

Monique Berthelon, Catherine Caillaud, Françoise Rey, Philippe Labrune, Dominique Melle, Josué Feingold, Jean Frézal, Marie-Louise Briard, Jean-Pierre Farriaux, Pierre Guibaud, Hubert Journel, Bernard

Journal:

Year:

1991

Language:

english

File:

PDF, 396 KB

english, 1991

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