(Q42456065)

31 October 2017

title

Germline PTCH1 mutations in Japanese basal cell nevus syndrome patients (English)

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31 October 2017

Chiaki Takahashi

1

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31 October 2017

Nozomi Kanazawa

2

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31 October 2017

Yoshie Yoshikawa

3

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31 October 2017

Reigetsu Yoshikawa

4

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31 October 2017

Yuko Saitoh

5

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31 October 2017

Hideaki Chiyo

6

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31 October 2017

Takakuni Tanizawa

7

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31 October 2017

Tomoko Hashimoto-Tamaoki

8

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31 October 2017

Yoshiro Nakano

9

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31 October 2017

publication date

26 June 2009

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Journal of Human Genetics

31 October 2017

published in

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31 October 2017

volume

54

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31 October 2017

issue

7

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31 October 2017

page(s)

403-408

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Nevoid basal-cell carcinoma syndrome

31 October 2017

cites work

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Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome

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Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

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Human homolog of patched, a candidate gene for the basal cell nevus syndrome

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7 January 2021

PTCH mutations: distribution and analyses

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Biochemical evidence that patched is the Hedgehog receptor

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The tumour-suppressor gene patched encodes a candidate receptor for Sonic hedgehog

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Malignant transformation and new primary tumours after therapeutic radiation for benign disease: substantial risks in certain tumour prone syndromes

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Mutations in the human homologue of Drosophila patched in Japanese nevoid basal cell carcinoma syndrome patients

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7 January 2021

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7 January 2021

Germline mutations of the PTCH gene in Japanese patients with nevoid basal cell carcinoma syndrome.

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7 January 2021

Naevoid basal cell carcinoma syndrome with a palmar epidermoid cyst, milia and maxillary cysts

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7 January 2021

A new germline mutation of the PTCH gene in a Japanese patient with nevoid basal cell carcinoma syndrome associated with meningioma

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7 January 2021

Detecting tissue-specific alternative splicing and disease-associated aberrant splicing of the PTCH gene with exon junction microarrays

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7 January 2021

Germline mutations of the PTCH gene in Japanese patients with nevoid basal cell carcinoma syndrome

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7 January 2021

Patched homologue 1 mutations in four Japanese families with basal cell nevus syndrome

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7 January 2021

New mutation of the PTCH gene in nevoid basal-cell carcinoma syndrome with West syndrome

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7 January 2021

A novel PTCH1 mutation in a patient of nevoid basal cell carcinoma syndrome

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7 January 2021

A novel germ-line mutation of PTCH1 gene in a Japanese family of nevoid basal cell carcinoma syndrome: are the palmoplantar pits associated with true basal cell carcinoma?

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7 January 2021

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7 January 2021

High-density oligonucleotide array with sub-kilobase resolution reveals breakpoint information of submicroscopic deletions in nevoid basal cell carcinoma syndrome

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7 January 2021

A missense mutation in PTCH2 underlies dominantly inherited NBCCS in a Chinese family

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7 January 2021

Alu repeats and human genomic diversity

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7 January 2021

The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors

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7 January 2021

Identifiers

DOI

10.1038/JHG.2009.55

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31 October 2017

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