Cargando…

Genetic aspects of a new mutation (S(al-s)) to sex-linked imperfect albinism in chickens

Detalles Bibliográficos
Autores principales:	Silversides, FG, Crawford, RD
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 1990
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2732683/ http://dx.doi.org/10.1186/1297-9686-22-4-447

Ejemplares similares

Prospective Study of the Phenotypic and Mutational Spectrum of Ocular Albinism and Oculocutaneous Albinism
por: Chan, Hwei Wuen, et al.
Publicado: (2021)

Albinism, Partial Albinism, and Vitiligo
por: Kugelman, Thomas P., et al.
Publicado: (1961)

A Molecular Link between Albinism and Visual Deficits
por: Gross, Liza
Publicado: (2008)

Genetic analyses of oculocutaneous albinism types 1 and 2 with four novel mutations
por: Yang, Qi, et al.
Publicado: (2019)

Molecular genetic and clinical evaluation of three Chinese families with X-linked ocular albinism
por: Zou, Xuan, et al.
Publicado: (2017)

Clinical and genetic variability in children with partial albinism
por: Campbell, Patrick, et al.
Publicado: (2019)

Genetic Causes of Oculocutaneous Albinism in Pakistani Population
por: Sajid, Zureesha, et al.
Publicado: (2021)

Genetic analyses of Vietnamese patients with oculocutaneous albinism
por: Thuong, Ma Thi Huyen, et al.
Publicado: (2022)

Oculocutaneous albinism
por: Grønskov, Karen, et al.
Publicado: (2007)

A new type of oculocutaneous albinism with a novel OCA2 mutation
por: Lee, Sang Yoon, et al.
Publicado: (2020)

Mutational Analysis of Oculocutaneous Albinism: A Compact Review
por: Kamaraj, Balu, et al.
Publicado: (2014)

Mutation analysis of a Chinese family with oculocutaneous albinism
por: Wang, Xiong, et al.
Publicado: (2016)

Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinism
por: Fang, Shaohua, et al.
Publicado: (2008)

Albinism: epidemiology, genetics, cutaneous characterization, psychosocial factors()()
por: Marçon, Carolina Reato, et al.
Publicado: (2019)

Albin, Vasconcelos, Elizondo
por: Albin Zychlisky, Enrique, 1954-
Publicado: (1995)

Albinism: Images in ophthalmology
por: Sreelatha, O. K., et al.
Publicado: (2009)

Albinism in barley androgenesis
por: Makowska, Katarzyna, et al.
Publicado: (2013)

Retinal detachment in albinism
por: Mansour, Ahmad M, et al.
Publicado: (2018)

A novel GPR143 mutation in a Chinese family with X-linked ocular albinism type 1
por: Gao, Xuhui, et al.
Publicado: (2020)

Occipital Petalia and Albinism: A Study of Interhemispheric VEP Asymmetries in Albinism with No Nystagmus
por: Liasis, Alkiviades, et al.
Publicado: (2019)

Living with albinism in an African community: exploring the challenges of persons with albinism in Lilongwe District, Malawi
por: Tambala-Kaliati, Thandiwe, et al.
Publicado: (2021)

A nonsense mutation in the tyrosinase gene causes albinism in water buffalo
por: Damé, Maria Cecília Florisbal, et al.
Publicado: (2012)

Mutational analysis of a Chinese family with oculocutaneous albinism type 2
por: Wang, Xiong, et al.
Publicado: (2017)

GPR143 mutations in Chinese patients with ocular albinism type 1
por: Jia, Xiuhua, et al.
Publicado: (2017)

Nonhuman Primate Model of Oculocutaneous Albinism with TYR and OCA2 Mutations
por: Wu, Kun-Chao, et al.
Publicado: (2020)

The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences
por: Kruijt, Charlotte C., et al.
Publicado: (2022)

Albinism in US Charolais cattle
por: Jayasekera, U, et al.
Publicado: (1981)

Retinopathy of prematurity in oculocutaneous albinism
por: Chandra, Parijat, et al.
Publicado: (2019)

The Coexistence of Oculocutaneous Albinism with Schizophrenia
por: Tsai, Alicia L, et al.
Publicado: (2020)

Photosensitivity and filter efficacy in albinism(✰)
por: Hansen, Tanja B., et al.
Publicado: (2023)

Molecular genetic studies and delineation of the oculocutaneous albinism phenotype in the Pakistani population
por: Jaworek, Thomas J, et al.
Publicado: (2012)

Genetic analysis and prenatal diagnosis of 20 Chinese families with oculocutaneous albinism
por: Xu, Chenyang, et al.
Publicado: (2020)

Genetic Analysis of 28 Chinese Families With Tyrosinase-Positive Oculocutaneous Albinism
por: Ma, Linya, et al.
Publicado: (2021)

Insights into the physiological, molecular, and genetic regulators of albinism in Camellia sinensis leaves
por: Zhao, Yang, et al.
Publicado: (2023)

Albinism in the domestic cat (Felis catus) is associated with a tyrosinase (TYR) mutation
por: Imes, DL, et al.
Publicado: (2006)

Eight previously unidentified mutations found in the OA1 ocular albinism gene
por: Mayeur, Hélène, et al.
Publicado: (2006)

Spectrum of candidate gene mutations associated with Indian familial oculocutaneous and ocular albinism
por: Renugadevi, Kathirvel, et al.
Publicado: (2010)

Albinism-Causing Mutations in Recombinant Human Tyrosinase Alter Intrinsic Enzymatic Activity
por: Dolinska, Monika B., et al.
Publicado: (2014)

Deep intronic GPR143 mutation in a Japanese family with ocular albinism
por: Naruto, Takuya, et al.
Publicado: (2015)

Imperfections in crystals
por: Van Bueren, Hendrik G
Publicado: (1961)

Cannot write session to /tmp/vufind_sessions/sess_6pgi91qohu15di9kn0rjb5e9qr