A new set of primers for mutation analysis of the human PAX6 gene.
about
Pax6 3' deletion results in aniridia, autism and mental retardationThree novel PAX6 mutations in patients with aniridia.Mutation analysis of PAX6 in inherited and sporadic aniridia from northeastern ChinaMolecular analysis of the PAX6 gene in Mexican patients with congenital aniridia: report of four novel mutations.Assessment of PAX6 alleles in 66 families with aniridia.Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalitiesPAX6, paired domain influences sequence recognition by the homeodomain.PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation.Mutation in the PAX6 gene in twenty patients with aniridia.Familial Limbal Stem Cell Deficiency: Clinical, Cytological and Genetic Characterization.
P2860
Q24658076-32257FD4-EBC5-4CDB-BB78-D70C4BD17203Q30320660-5E432EE8-ED7D-4564-8180-2E409FA036F3Q36099716-A896B74D-65AC-40A4-B93A-7C00BD341246Q36864284-7AF15756-06EA-4BB8-8BEA-4DB286108E33Q36918047-23E0EDD1-BD89-498F-BA51-2EAAE342429CQ41979823-024A6FF4-235B-497D-9AF3-C38CB1DE8FC7Q42809226-AB907529-7860-4645-9B8D-3540A73D2550Q43734716-5E5F0043-D463-4CB8-8324-5EF1D13154FCQ47873930-CF92D647-25D4-4185-B456-975E2ADBA3E4Q48310555-DD979290-D1F7-42DD-8806-F3CE5304C5A0
P2860
A new set of primers for mutation analysis of the human PAX6 gene.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh
1998年學術文章
@zh-hant
name
A new set of primers for mutation analysis of the human PAX6 gene.
@en
type
label
A new set of primers for mutation analysis of the human PAX6 gene.
@en
prefLabel
A new set of primers for mutation analysis of the human PAX6 gene.
@en
P2093
P2860
P1433
P1476
A new set of primers for mutation analysis of the human PAX6 gene.
@en
P2093
P2860
P304
P356
10.1002/(SICI)1098-1004(1998)12:2<128::AID-HUMU8>3.0.CO;2-N
P577
1998-01-01T00:00:00Z