A novel deletion in exon 15 of the adenomatous polyposis coli gene in an Italian kindred-Reference-Cited by-同舟云学术

A novel deletion in exon 15 of the adenomatous polyposis coli gene in an Italian kindred

Published:1994 Issue:3 Volume:3 Page:301-304
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Cama Alessandro,Palmirotta Raffaele,Esposito Diana,Curia Maria Cristina,Ranieri Annalisa,Ficari Ferdinando,Valanzano Rosa,Battista Pasquale,Frati Luigi,Tonelli Francesco,Mariani-Costantini Renato

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference18 articles.

1. Hyperpigmented lesions of the retinal pigment epithelium in familial adenomatous polyposis

2. The UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculations.

3. The Amino Acid Sequence of the Insulin Receptor Is Normal in an Insulin-Resistant Pima Indian*

4. A Mutation in the Tyrosine Kinase Domain of the Insulin Receptor Associated with Insulin Resistance in an Obese Woman*

5. Molecular analysis of APC mutations in familial adenomatous polyposis and sporadic colon carcinomas

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1. Heteroduplex Analysis of Causative APC Mutations in FAP Patients Referred for Genetic Counseling in Mashhad Ghaem Hospital, Iran;Shiraz E-Medical Journal;2013-10-01

2. Thyroid Carcinoma Usually Occurs in Patients with Familial Adenomatous Polyposis in the Absence of Biallelic Inactivation of the Adenomatous Polyposis Coli Gene;Journal of Clinical Endocrinology & Metabolism;2001-01-01

3. Germline Mutations of the APC Gene in Patients with Familial Adenomatous Polyposis-Associated Thyroid Carcinoma: Results from a European Cooperative Study;Journal of Clinical Endocrinology & Metabolism;2000-01-01

4. Optimized PCR labeling in mutational and microsatellite analysis;Clinical Chemistry;1998-07-01

5. Novel allele of the insulin receptor substrate‐1 bearing two non‐conservative amino acid substitutions in a patient with noninsulin‐dependent diabetes mellitus;Human Mutation;1998-01