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X
Briard, Marie-Louise
43  Ergebnisse:
Personensuche X
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1

Nance-Horan syndrome: linkage analysis in 4 families refine..:

Toutain, A. ; Ronce, Nathalie ; Dessay, Benoît...
Human Genetics.  99 (1997)  2 - p. 256-261 , 1997
Link: https://doi.org/10.1007/..
 
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2

A gene for Leber's congenital amaurosis maps to chromosome ..:

Camuzat, Agnès ; Dollfus, Hélène ; Rozet, Jean-Michel...
Human Molecular Genetics.  4 (1995)  8 - p. 1447-1452 , 1995
Link: https://doi.org/10.1093/..
 
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3

A gene for Stargardt's disease (fundus flavimaculatus) maps..:

Kaplan, Josseline ; Gerber, Sylvie ; Larget-Piet, Dominique...
Nature Genetics.  5 (1993)  3 - p. 308-311 , 1993
Link: https://doi.org/10.1038/..
 
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4

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

Lyonnet, Stanislas ; Pelet, Anna ; Royer, Ghislaine...
Genomics.  14 (1992)  2 - p. 508-510 , 1992
Link: https://doi.org/10.1016/..
 
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5

Linkage disequilibrium between phenylketonuria and RFLP hap..:

Caillaud, Catherine ; Vilarinho, Laura ; Vilarinho, Antoine...
Human Genetics.  89 (1992)  1 - p. 69-72 , 1992
Link: https://doi.org/10.1007/..
 
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6

Spectrum of phenylketonuria mutations in Western Europe and..:

Berthelon, Monique ; Caillaud, Catherine ; Rey, Françoise...
Human Genetics.  86 (1991)  4 - p. 355-358 , 1991
Link: https://doi.org/10.1007/..
 
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7

Neonatal myasthenia gravis:

Morel, Evelyne ; Bach, Jean-François ; Briard, Marie-Louise.
Journal of Neuroimmunology.  6 (1984)  5 - p. 313-317 , 1984
Link: https://doi.org/10.1016/..
 
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8

Embryonic testicular regression syndrome: Variable phenotyp..:

Josso, Nathalie ; Briard, Marie-Louise
The Journal of Pediatrics.  97 (1980)  2 - p. 200-204 , 1980
Link: https://doi.org/10.1016/..
 
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9

Congenital glaucoma: Genetic models:

Demenais, Florence ; Bona�ti, Catherine ; Briard, Marie-Louise..
Human Genetics.  46 (1979)  3 - p. 305-317 , 1979
Link: https://doi.org/10.1007/..
 
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10

Consanguinity in Multifactorial Inheritance: Application to..:

Bonaïti, Catherine ; Demenais, Florence ; Briard, Marie-Louise.
Human Heredity.  28 (1978)  5 - p. 361-371 , 1978
Link: https://www.jstor.org/st..
 
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11

Consanguinity in Multifactorial Inheritance:

Bonaïti, Catherine ; Demenais, Florence ; Briard, Marie-Louise.
Human Heredity.  28 (1978)  5 - p. 361-371 , 1978
Link: https://doi.org/10.1159/..
 
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12

Parental age in retinoblastoma:

Pelli�, Catherine ; Briard, Marie-Louise ; Feingold, Josu�.
Human Genetics.  20 (1973)  1 - p. 59-62 , 1973
Link: https://doi.org/10.1007/..
 
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13

Ethical aspects of neonatal screening for sickle cell disea..:

Montalembert, Mariane ; Bonnet, Doris ; Lena-Russo, Danielle.
Acta Paediatrica.  94 (2007)  5 - p. 528-530 , 2007
Link: https://doi.org/10.1111/..
 
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14

Segregation analysis in hereditary retinoblastoma:

Bona�ti-Pelli�, Catherine ; Briard-Guillemot, Marie Louise
Human Genetics.  57 (1981)  4 - p. 411-419 , 1981
Link: https://doi.org/10.1007/..
 
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15

Sister chromatid exchanges in patients with retinoblastoma:

Der-Sarkissian, Hera ; Bonaïti-Pellié, Catherine ; Briard-Guillemot, Marie-Louise.
Cancer Genetics and Cytogenetics.  7 (1982)  1 - p. 73-77 , 1982
Link: https://doi.org/10.1016/..
 
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