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Molecular Vision
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January 5, 2011
Mutations in the LHX2 gene are not a frequent cause of micro/anophthalmia
Annaïck Desmaison, Adeline Vigouroux, Claudine Rieubland, et al.
American Journal of Medical Genetics. Part A
|
August 19, 2003
Donnai-Barrow syndrome: four additional patients
Nicolas Chassaing, Didier Lacombe, Dominique Carles, et al.
Molecular Vision
|
January 6, 2009
Linkage analysis of high myopia susceptibility locus in 26 families
Sandrine Paget, Sophie Julia, Zulma G Vitezica, et al.
Ophthalmology
|
May 3, 2006
Corneal ectasia after photorefractive keratectomy for low myopia
François Malecaze, Julien Coullet, Patrick Calvas, et al.
Plos One
|
July 8, 2009
Quality of DNA extracted from mouthwashes
Tetyana Zayats, Terri L Young, David A Mackey, et al.
American Journal of Ophthalmology
|
January 5, 2005
Variable phenotype related to a novel PAX 6 mutation (IVS4+5G>C) in a family presenting congenital nystagmus and foveal hypoplasia
Marie-Claire Vincent, Raffaella Gallai, David Olivier, et al.
Clinical Case Reports
|
September 25, 2015
Double deletion of a chromosome 21 inserted in a chromosome 22 in an azoospermic patient
Valentine Marquet, Dominique Bourgeois, Philippe De Mas, et al.
Investigative Ophthalmology & Visual Science
|
October 11, 2012
A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population
Weihua Meng, Jacqueline Butterworth, Declan T Bradley, et al.
The Journal of Investigative Dermatology
|
April 17, 2004
Novel ABCC6 mutations in pseudoxanthoma elasticum
Nicolas Chassaing, Ludovic Martin, Juliette Mazereeuw, et al.
Journal of Health Psychology
|
November 12, 2019
Attitudes of French populations towards the disclosure of unsolicited findings in medical genetics
Marion Rosier, Myriam Guedj, Patrick Calvas, et al.
Page
of 10
Search research articles
Search
Showing results (11-20 of 97) with videos related to
Sort By:
Page
of 10
Molecular Vision
|
January 5, 2011
Mutations in the LHX2 gene are not a frequent cause of micro/anophthalmia
Annaïck Desmaison, Adeline Vigouroux, Claudine Rieubland, et al.
American Journal of Medical Genetics. Part A
|
August 19, 2003
Donnai-Barrow syndrome: four additional patients
Nicolas Chassaing, Didier Lacombe, Dominique Carles, et al.
Molecular Vision
|
January 6, 2009
Linkage analysis of high myopia susceptibility locus in 26 families
Sandrine Paget, Sophie Julia, Zulma G Vitezica, et al.
Ophthalmology
|
May 3, 2006
Corneal ectasia after photorefractive keratectomy for low myopia
François Malecaze, Julien Coullet, Patrick Calvas, et al.
Plos One
|
July 8, 2009
Quality of DNA extracted from mouthwashes
Tetyana Zayats, Terri L Young, David A Mackey, et al.
American Journal of Ophthalmology
|
January 5, 2005
Variable phenotype related to a novel PAX 6 mutation (IVS4+5G>C) in a family presenting congenital nystagmus and foveal hypoplasia
Marie-Claire Vincent, Raffaella Gallai, David Olivier, et al.
Clinical Case Reports
|
September 25, 2015
Double deletion of a chromosome 21 inserted in a chromosome 22 in an azoospermic patient
Valentine Marquet, Dominique Bourgeois, Philippe De Mas, et al.
Investigative Ophthalmology & Visual Science
|
October 11, 2012
A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population
Weihua Meng, Jacqueline Butterworth, Declan T Bradley, et al.
The Journal of Investigative Dermatology
|
April 17, 2004
Novel ABCC6 mutations in pseudoxanthoma elasticum
Nicolas Chassaing, Ludovic Martin, Juliette Mazereeuw, et al.
Journal of Health Psychology
|
November 12, 2019
Attitudes of French populations towards the disclosure of unsolicited findings in medical genetics
Marion Rosier, Myriam Guedj, Patrick Calvas, et al.
Page
of 10