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[A novel mutation in Mitf gene leads to a patient with Waardenburg syndrome type II].

Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery - 1 Oct 2007

Feng Yong, Liu Zheng-zheng, Hu Hao

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PMID: 18229597

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Related research

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Research trail→

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[A novel mutation in Mitf gene leads to a patient with Waardenburg syndrome type II].PMID 18229597Read ↗

A novel MITF splice site mutation in a family with Waardenburg syndrome.Semantic proximity Read ↗

[Study of gene mutation and pathogenetic mechanism for a family with Waardenburg syndrome].Semantic proximity Read ↗

[Gene responsible for Waardenburg syndrome type I].Semantic proximity Read ↗

[Clinical classification and genetic mutation study of two pedigrees with type II Waardenburg syndrome].Semantic proximity Read ↗

A new 3p interstitial deletion including the entire MITF gene causes a variation of Tietz/Waardenburg type IIA syndromes.Semantic proximity Read ↗

[Application of next generation sequencing in 3 Waardenburg syndrome].Semantic proximity Read ↗

[Mutation analysis of seven patients with Waardenburg syndrome].Semantic proximity Read ↗

[Mutation screening of MITF gene in patients with Waardenburg syndrome type 2].Semantic proximity Read ↗

Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation.Semantic proximity Read ↗

[Waardenburg syndrome].Semantic proximity Read ↗

[Still disease with heterozygous MEFV mutation].Semantic proximity Read ↗

Frameshift variant in MITF gene in a large family with Waardenburg syndrome type II and a co-segregation of a C2orf74 variant.Semantic proximity Read ↗

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