Analysis of recurrent germline mutations in the MEN1 gene encountered in apparently unrelated families (Q47815031)

5 February 2018

title

Analysis of recurrent germline mutations in the MEN1 gene encountered in apparently unrelated families (English)

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5 February 2018

14

Collins FS

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author name string

Agarwal SK

1

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5 February 2018

Debelenko LV

2

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5 February 2018

Kester MB

3

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Guru SC

4

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5 February 2018

Manickam P

5

1 reference

5 February 2018

Olufemi SE

6

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5 February 2018

Skarulis MC

7

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5 February 2018

Heppner C

8

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5 February 2018

Crabtree JS

9

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5 February 2018

Lubensky IA

10

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5 February 2018

Zhuang Z

11

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5 February 2018

Kim YS

12

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Chandrasekharappa SC

13

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Liotta LA

15

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Spiegel AM

16

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Burns AL

17

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Emmert-Buck MR

18

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Marx SJ

19

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5 February 2018

publication date

1 January 1998

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5 February 2018

published in

Human Mutation

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5 February 2018

volume

12

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5 February 2018

issue

2

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5 February 2018

page(s)

75-82

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5 February 2018

The pattern of spontaneous germ-line mutation: relative rates of mutation at or near CpG dinucleotides in the factor IX gene

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Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene

21 January 2018

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Positional cloning of the gene for multiple endocrine neoplasia-type 1

21 January 2018

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CpNpG methylation in mammalian cells

21 January 2018

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Laser capture microdissection

21 January 2018

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Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1

21 January 2018

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Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1

21 January 2018

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A 2.8-Mb clone contig of the multiple endocrine neoplasia type 1 (MEN1) region at 11q13.

21 January 2018

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Somatic mutation of the MEN1 gene in parathyroid tumours

21 January 2018

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Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment

21 January 2018

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Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma

21 January 2018

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Constitutively methylated CpG dinucleotides as mutation hot spots in the retinoblastoma gene (RB1).

21 January 2018

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Eighteen new polymorphic markers in the multiple endocrine neoplasia type 1 (MEN1) region

21 January 2018

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Genetic aspects of adenomatosis of endocrine glands

21 January 2018

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Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states

21 January 2018

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Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11

21 January 2018

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Loss of heterozygosity at 11q13: analysis of pituitary tumors, lung carcinoids, lipomas, and other uncommon tumors in subjects with familial multiple endocrine neoplasia type 1

21 January 2018

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DNA methylation and cancer

21 January 2018

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Homonucleotide tracts, short repeats and CpG/CpNpG motifs are frequent sites for heterogeneous mutations in the neurofibromatosis type 1 (NF1) tumour-suppressor gene

21 January 2018

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Large majority of single-nucleotide mutations along the dystrophin gene can be explained by more than one mechanism of mutagenesis

21 January 2018

1 reference

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10.1002/(SICI)1098-1004(1998)12:2<75::AID-HUMU1>3.0.CO;2-T

21 January 2018

Identifiers

DOI

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5 February 2018

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5 February 2018