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A mutation screen of Exons 3 and 4 was negative.
No targeted mutation screen of NDN has previously been performed in human cancer.
We performed a mutation screen of the coding region of SH2B1 in 95 extremely obese children and adolescents.
The mutation screen of 175 cases identified one deleterious nonsense mutation, p.Arg186* (c.556C>T), in a Canadian family.
Taken together, our mutation screen of uterine leiomyomas did not reveal somatic coding mutations in CDK8/ CCNC9, CCNC, and MED13.
The partial mutation screen of exons 2, 13, and 22 identified three distinct mutations in healthy women, including c.68_69delAG, c.4327C>T, and c.5454delC [ 18].
Similar(48)
Mutation screening of the phosducin gene PDC in patients with retinitis pigmentosa and allied diseases.
Mutation screening of the NBS1 gene was carried out to confirm the diagnosis in 7 cases.
Accordingly, our results pave the way for potentially less invasive mutation screening of MM patients through characterization of CTCs.
Mutation screening of the peropsin gene, a retinal pigment epithelium specific rhodopsin homolog, in patients with retinitis pigmentosa and allied diseases.
We designed mutation screening of exon 5 of CHRNA4, exon 5 of CHRNB2, and exon 6 of CHRNA2 in a group of 56 Chinese sporadic NFLE cases.
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