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Search for publications relevant for "exon 16"
exon 16
Publication
Class
Person
Publication
Programmes
publication
The newly detected mutations in the RET proto-oncogene in exon 16 as a cause of sporadic medullary thyroid carcinoma
2003 |
Second Faculty of Medicine
publication
Double Germline Mutations in the RET Proto-oncogene in MEN 2A and MEN 2B Kindreds
2006 |
Publication without faculty affiliation
publication
Double Germline Mutations in the RET Proto-oncogene in MEN 2A and MEN 2B Kindreds
2006 |
First Faculty of Medicine
publication
New multiple somatic mutations in the RET proto-oncogene associated with a sporadic medullary thyroid carcinoma
2007 |
First Faculty of Medicine
publication
Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinomas
2008 |
Faculty of Medicine in Hradec Králové
publication
Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinomas
2008 |
First Faculty of Medicine
publication
Paraganglioma-like medullary thyroid carcinoma: fine needle aspiration cytology features with histological correlation
2009 |
Faculty of Medicine in Hradec Králové
publication
New multiple somatic mutations in the RET proto-oncogene associated with a sporadic medullary thyroid carcinoma
2006 |
Central Library of Charles University, First Faculty of Medicine
publication
New multiple somatic mutations in the RET proto-oncogene associated with a sporadic medullary thyroid carcinoma
2006 |
Second Faculty of Medicine
publication
New multiple somatic mutations in the RET proto-oncogene associated with a sporadic medullary thyroid carcinoma
2006 |
Faculty of Medicine in Hradec Králové, Central Library of Charles University, First Faculty of Medicine, Second Faculty of Medicine
publication
Paraganglioma-like medullary thyroid carcinoma: fine needle aspiration cytology features with histological correlation
+1
2009 |
Faculty of Medicine in Hradec Králové, Central Library of Charles University
publication
Paraganglioma-like medullary thyroid carcinoma: fine needle aspiration cytology features with histological correlation
2009 |
First Faculty of Medicine
publication
Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinomas
2008 |
Faculty of Medicine in Hradec Králové, Central Library of Charles University
publication
Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinomas
2008 |
Faculty of Medicine in Hradec Králové, Central Library of Charles University, First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinomas
2008 |
Second Faculty of Medicine
publication
Double Germline Mutations in the RET Proto-oncogene in MEN 2A and MEN 2B Kindreds
2006 |
Faculty of Medicine in Hradec Králové, Central Library of Charles University
publication
The human cystathionine beta-synthase (CBS) gene: Complete sequence, alternative splicing, and polymorphisms
1998 |
Faculty of Physical Education and Sport
publication
Double germline mutations in the RET proto-oncogene in MEN 2A and MEN 2B kindreds
2006 |
Second Faculty of Medicine
publication
Double Germline Mutations in the RET Proto-oncogene in MEN 2A and MEN 2B Kindreds
2006 |
Faculty of Medicine in Hradec Králové, Central Library of Charles University, First Faculty of Medicine, Second Faculty of Medicine
publication
Detection of two Alu insertions in the CFTR gene
2008 |
Second Faculty of Medicine
publication
RET mutation Tyr791Phe: the genetic cause of different diseases derived from neural crest
2009 |
Second Faculty of Medicine
publication
RET mutation Tyr791Phe: the genetic cause of different diseases derived from neural crest
2009 |
Central Library of Charles University, First Faculty of Medicine, Second Faculty of Medicine
publication
Screening of six risk exons of the RET proto-oncogene in families with medullary thyroid carcinoma in the Czech Republic
2004 |
Second Faculty of Medicine
publication
First Report of Recurrent Nephrotic Syndrome After Kidney Transplantation in a Patient With NUP93 Gene Mutations: A Case Report
2018 |
Second Faculty of Medicine, Faculty of Medicine in Pilsen