نتایج جستجو برای: oca1a albinism

تعداد نتایج: 7091  

Journal: :Journal of medical genetics 1976
W G Pearce R Sanger

A Newfoundland kindred in which ocular albinism and deutan colour blindness are segregating provides strong evidence against the loci for these two X-borne characters being within direct measurable distance of each other.

2015
Valentina Cetica Yvonne Hackmann Samantha Grieve Elena Sieni Benedetta Ciambotti Maria Luisa Coniglio Daniela Pende Kimberly Gilmour Paolo Romagnoli Gillian M. Griffiths Maurizio Aricò

BACKGROUND Familial hemophagocytic lymphohistiocytosis (FHL) is a rare and often fatal disorder characterized by defective cellular cytotoxicity and hyperinflammation, and the only cure known to date is hematopoietic stem cell transplantation. Mutations in RAB27A, LYST, and AP3B1 give rise to FHL associated with oculocutaneous albinism, and patients with FHL are usually only screened for mutati...

Journal: :Molecular vision 2007
Markus N Preising Hedwig Forster H Tan Birgit Lorenz Paulus T V M de Jong Astrid S Plomp

PURPOSE To elucidate the molecular basis of oculocutaneous albinism with variable expressivity in a family from The Netherlands in which no consanguinity was reported. METHODS Three affected family members were screened for mutations in tyrosinase (TYR) and the pink-eye-dilution gene (P) by using SSCP. The melanocortin receptor gene (MC1R) and amplimers of P showing an aberrant banding patter...

Journal: :gene, cell and tissue 0
farah talebi milad genetic counseling center, ahvaz, ir iran farideh ghanbari department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, ir iran; department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, ir iran. tel/fax: +98-6136233884 javad mohammadi asl department of medical genetics, faculty of medicine, ahvaz jundishapur university of medical sciences, ahvaz, ir iran

introduction oculocutaneous albinism (oca) is a genetically heterogeneous autosomal recessive genetic disorder that is characterized by reduced or completely absent pigmentation in the hair, skin, and eyes. conclusions a novel homozygous mutation, the deletion of exons 1 - 5 on the tyr gene, was found on the molecular genetic testing of this patient. exon 1 - 5 deletion on tyr causes a lack of ...

Journal: :The British journal of ophthalmology 1985
P E Kinnear E G Tuddenham

Four cases of albinism with haemorrhagic diathesis (Hermansky-Pudlak syndrome) are presented. The cases displayed wide phenotypic variation. Electroretinography was performed on all four patients and was found to be normal. One patient developed a cutaneous malignant melanoma.

Journal: :Genetics Selection Evolution 1981

Journal: :Annals of Eugenics 1953

2016
Linda K. McLoon Christy L. Willoughby Jill S. Anderson Erick D. Bothun David Stager Joost Felius Helena Lee Irene Gottlob

PURPOSE Infantile nystagmus syndrome (INS) is often associated with abnormalities of axonal outgrowth and connectivity. To determine if this manifests in extraocular muscle innervation, specimens from children with idiopathic INS or INS and albinism were examined and compared to normal age-matched control extraocular muscles. METHODS Extraocular muscles removed during normal surgery on childr...

Journal: :Biocatalysis and agricultural biotechnology 2021

Rice plant regeneration via anther culture possess several difficulties, these included early necrosis and high albinism frequency. In the present study, biotic abiotic factors were studied to develop an efficient protocol for of Malaysian indica rice MR 219 variety. Callus initiation cultures was evaluated using different N6 media supplemented with 2,4-D in combination 1-naphthaleneacetic acid...

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