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	1.	Mapping of the X-linked recessive retinitis pigmentosa gene. A review. [electronic resource] by Musarella, M A Producer: 19900831 In: Ophthalmic paediatrics and genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Patient with Bardet-Biedl syndrome presenting with nystagmus at fifteen months of age. [electronic resource] by Musarella, M A Producer: 20011204 In: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Gene mapping of ocular diseases. [electronic resource] by Musarella, M A Producer: 19920423 In: Survey of ophthalmology vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Molecular genetics of macular degeneration. [electronic resource] by Musarella, M A Producer: 20020115 In: Documenta ophthalmologica. Advances in ophthalmology vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Genetic counseling in X-linked retinitis pigmentosa. [electronic resource] by Anandakrishnan, I Musarella, M A Producer: 19890707 In: Journal of pediatric ophthalmology and strabismus vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	An infant with Turner-Down aneuploidy and massive capillary hemangioma of the orbit: a case report with review. [electronic resource] by Musarella, M A Verma, R S Producer: 20011204 In: Annales de genetique vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A patient with median cleft face anomaly and bilateral Goldenhar anomaly. [electronic resource] by Musarella, M A Young, I D Producer: 19890323 In: American journal of medical genetics. Supplement vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A simplified scheme for genetic counseling in retinoblastoma. [electronic resource] by Musarella, M A Gallie, B L Producer: 19870811 In: Journal of pediatric ophthalmology and strabismus vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Primary angle closure glaucoma and retinitis pigmentosa. [electronic resource] by Badeeb, O Trope, G Musarella, M Producer: 19940506 In: Acta ophthalmologica vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Anterior segment and intraocular pressure measurements of the unanesthetized premature infant. [electronic resource] by Musarella, M A Morin, J D Producer: 19880712 In: Metabolic, pediatric, and systemic ophthalmology (New York, N.Y. : 1985) vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	11.	Clinical spectrum of leber's congenital amaurosis in the second to fourth decades of life. [electronic resource] by Smith, D Oestreicher, J Musarella, M A Producer: 19901205 In: Ophthalmology vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	A nonsense mutation in the tyrosinase gene of Afghan patients with tyrosinase negative (type IA) oculocutaneous albinism. [electronic resource] by Giebel, L B Musarella, M A Spritz, R A Producer: 19911021 In: Journal of medical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Summary of ocular genetic disorders and inherited systemic conditions with eye findings. [electronic resource] by MacDonald, I M Haney, P M Musarella, M A Producer: 19980717 In: Ophthalmic genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Ocular involvement in neuroblastoma: prognostic implications. [electronic resource] by Musarella, M A Chan, H S DeBoer, G Gallie, B L Producer: 19841128 In: Ophthalmology vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosa. [electronic resource] by Riess, O Noerremoelle, A Weber, B Musarella, M A Hayden, M R Producer: 19921028 In: American journal of human genetics vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	16.	The optic disc in Leber congenital amaurosis. [electronic resource] by Sullivan, T J Lambert, S R Buncic, J R Musarella, M A Producer: 19921001 In: Journal of pediatric ophthalmology and strabismus vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Dinucleotide repeat polymorphism near the RP3 locus in Xp21 (DXS1110). [electronic resource] by Roux, A F Yuan, C C Rommens, J M Musarella, M A Producer: 19930921 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	The ocular pathology in Leber's congenital amaurosis. [electronic resource] by Sullivan, T J Heathcote, J G Brazel, S M Musarella, M A Producer: 19940825 In: Australian and New Zealand journal of ophthalmology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Dinucleotide repeat polymorphism at the human recoverin RCVI gene locus on chromosome 17p. [electronic resource] by Dollfus, H Rozet, J M Musarella, M A Kaplan, J Munnich, A Producer: 19931004 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	First African-American child with juvenile neuronal ceroid lipofuscinosis. [electronic resource] by Inan, C Wong, D Wisniewski, K E Rose, A L Musarella, M A Producer: 19990602 In: American journal of medical genetics vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 47 results.