Your search returned 56 results.

Results
	1.	Gene discovery and prevalence in inherited retinal dystrophies. [electronic resource] by Hamel, Christian P Producer: 20141117 In: Comptes rendus biologies vol. 337 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Cone rod dystrophies. [electronic resource] by Hamel, Christian P Producer: 20071106 In: Orphanet journal of rare diseases vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	[Inherited retinal dystrophies: contributions of molecular genetics]. [electronic resource] by Hamel, Christian P Producer: 20140701 In: Biologie aujourd'hui vol. 207 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Clinical utility gene card for: blue cone monochromatism. [electronic resource] by Kohl, Susanne Hamel, Christian P Producer: 20110913 In: European journal of human genetics : EJHG vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Clinical utility gene card for: achromatopsia. [electronic resource] by Kohl, Susanne Hamel, Christian P Producer: 20110913 In: European journal of human genetics : EJHG vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Choroideremia: towards a therapy. [electronic resource] by Kalatzis, Vasiliki Hamel, Christian P MacDonald, Ian M Producer: 20131115 In: American journal of ophthalmology vol. 156 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	How can we prevent myopia progression? [electronic resource] by Chassine, Thomas Villain, Max Hamel, Christian P Daien, Vincent Producer: 20150921 In: European journal of ophthalmology vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Gene structure and chromosomal localization of mouse Opa1 : its exclusion from the Bst locus. [electronic resource] by Delettre, Cécile Lenaers, Guy Belenguer, Pascale Hamel, Christian P Producer: 20040610 In: BMC genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Identification of preferentially expressed mRNAs in retina and cochlea. [electronic resource] by Maubaret, Cécilia Delettre, Cécile Sola, Sandrine Hamel, Christian P Producer: 20030115 In: DNA and cell biology vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	RRH, encoding the RPE-expressed opsin-like peropsin, is not mutated in retinitis pigmentosa and allied diseases. [electronic resource] by Ksantini, Mohamed Sénéchal, Audrey Humbert, Ghyslaine Arnaud, Bernard Hamel, Christian P Producer: 20070522 In: Ophthalmic genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosa. [electronic resource] by Ksantini, Mohamed Lafont, Estèle Bocquet, Béatrice Meunier, Isabelle Hamel, Christian P Producer: 20121004 In: European journal of ophthalmology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	OPA1 (Kjer type) dominant optic atrophy: a novel mitochondrial disease. [electronic resource] by Delettre, Cécile Lenaers, Guy Pelloquin, Laeticia Belenguer, Pascale Hamel, Christian P Producer: 20020521 In: Molecular genetics and metabolism vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Screening genes of the visual cycle RGR, RBP1 and RBP3 identifies rare sequence variations. [electronic resource] by Ksantini, Mohamed Sénéchal, Audrey Bocquet, Béatrice Meunier, Isabelle Brabet, Philippe Hamel, Christian P Producer: 20110121 In: Ophthalmic genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Lack of fundus autofluorescence to 488 nanometers from childhood on in patients with early-onset severe retinal dystrophy associated with mutations in RPE65. [electronic resource] by Lorenz, Birgit Wabbels, Bettina Wegscheider, Erika Hamel, Christian P Drexler, Wolfgang Preising, Markus N Producer: 20040810 In: Ophthalmology vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Simple and efficient: validation of a cotton wick electrode for animal electroretinography. [electronic resource] by Chekroud, Karim Arndt, Carl Basset, Danièle Hamel, Christian P Brabet, Philippe Pequignot, Marie O Producer: 20110825 In: Ophthalmic research vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Early-onset foveal involvement in retinitis punctata albescens with mutations in RLBP1. [electronic resource] by Dessalces, Elodie Bocquet, Béatrice Bourien, Jérôme Zanlonghi, Xavier Verdet, Robert Meunier, Isabelle Hamel, Christian P Producer: 20131210 In: JAMA ophthalmology vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Screening for a canine model of choroideremia exclusively identifies nonpathogenic CHM variants. [electronic resource] by Robert, Lorenne Sénéchal, Audrey Bocquet, Béatrice Herbin, Laetitia Chaudieu, Gilles Kalatzis, Vasiliki André, Catherine Hamel, Christian P Producer: 20110622 In: Ophthalmic research vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Homozygosity mapping in autosomal recessive retinitis pigmentosa families detects novel mutations. [electronic resource] by Bocquet, Béatrice Marzouka, Nour Al Dain Hebrard, Maxime Manes, Gaël Sénéchal, Audrey Meunier, Isabelle Hamel, Christian P Producer: 20140721 In: Molecular vision vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	19.	A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunit. [electronic resource] by Manes, Gaël Cheguru, Pallavi Majumder, Anurima Bocquet, Béatrice Sénéchal, Audrey Artemyev, Nikolai O Hamel, Christian P Brabet, Philippe Producer: 20150109 In: PloS one vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Homozygous deletion related to Alu repeats in RLBP1 causes retinitis punctata albescens. [electronic resource] by Humbert, Ghyslaine Delettre, Cécile Sénéchal, Audrey Bazalgette, Cécile Barakat, Abdelhamid Bazalgette, Christian Arnaud, Bernard Lenaers, Guy Hamel, Christian P Producer: 20061208 In: Investigative ophthalmology & visual science vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

1
2
3
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 56 results.