Genetic Counselor Practices Involving Pediatric Patients with FAP: an Investigation of their Self-Reported Strategies for Genetic Testing and Hepatoblastoma Screening.

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Genetic Counselor Practices Involving Pediatric Patients with FAP: an Investigation of their Self-Reported Strategies for Genetic Testing and Hepatoblastoma Screening.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

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name

Genetic Counselor Practices In ...... and Hepatoblastoma Screening.

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Genetic Counselor Practices In ...... and Hepatoblastoma Screening.

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Item

label

Genetic Counselor Practices In ...... and Hepatoblastoma Screening.

@en

Genetic Counselor Practices In ...... and Hepatoblastoma Screening.

@nl

prefLabel

Genetic Counselor Practices In ...... and Hepatoblastoma Screening.

@en

Genetic Counselor Practices In ...... and Hepatoblastoma Screening.

@nl

P1476

Genetic Counselor Practices In ...... g and Hepatoblastoma Screening

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P2093

Caitlin E Lawson

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Hongying Dai

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Seth Septer

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P2860

Desmoid tumors in a dutch cohort of patients with familial adenomatous polyposis

Familial adenomatous polyposis in two brothers with hepatoblastoma: implications for diagnosis and screening

Risk factors predicting desmoid occurrence in patients with familial adenomatous polyposis: a meta-analysis

Screening for Wilms tumor in children with Beckwith-Wiedemann syndrome or idiopathic hemihypertrophy.

Serum alpha-fetoprotein screening for hepatoblastoma in children with Beckwith-Wiedemann syndrome or isolated hemihyperplasia.

Parental attitudes, beliefs, and perceptions about genetic testing for FAP and colorectal cancer surveillance in minors.

Risk of hepatoblastoma in familial adenomatous polyposis.

Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?

Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.

Lack of association among typical congenital hypertrophy of the retinal pigment epithelium, adenomatous polyposis, and Gardner syndrome.

P304

586-593

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P31

scholarly article

P356

10.1007/S10897-016-0030-2

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P433

http://www.w3.org/2001/XMLSchema#string

P478

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P50

Thomas Attard

P577

2016-12-03T00:00:00Z

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P698

27913912

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