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proLékaře.cz / Journals / Clinical Oncology / 2009 - Supplementum

Commentary: Preimplantation Genetic Diagnosis

Czech version

Authors: doc. MUDr. Alice Baxová, CSc. 1;  prof. MUDr. Pavel Martásek, DrSc. 2
Authors‘ workplace: Ústav biologie a lékařské genetiky, 1. LFUK a VFN Praha 2Klinika dětského a dorostového lékařství 1. LF a VFN Praha 1
Published in: Klin Onkol 2009; 22(Supplementum): 75

Labels
Paediatric clinical oncology Surgery Clinical oncology
Hereditary Breast and Ovarian Cancer Syndrome
Hereditary Nonpolyposis Colorectal Cancer (HNPCC, Lynch syndrome)
Familial Adenomatous Polyposis
Li-Fraumeni Syndrome
Von Hippel-Lindau Disease
Multiple Endocrine Neoplasia Type 1 Syndrome
Multiple Endocrine Neoplasia Type 2 Syndrome
Familial Atypical Multiple Mole Melanoma Syndrome – FAMMM
Gorlin Syndrome
Peutz-Jeghers Syndrome
The Survey of Syndromes with the Risk of Cancer in Children Age
Tuberous Sclerosis
Hereditary Pancreatitis
Cowden Syndrome
Recommendation for Prophylactic Surgery for Decreasing the Risk of Gynaecological Cancer in Women with Hereditary Risk
Current Methods in Diagnostics and Monitoring of Patients with Hereditary Polyposis Syndromes. Investigation of the Small Intestine
Limitations of Genetic Testing in Oncology
Prerequisites for Preimplantation Genetic Diagnosis (PGD) in Carriers of Mutations Responsible for Hereditary Cancers
Commentary: The Possibilities of (Assisted Reproduction Techniques) in Control of Risk Genes Transfer to the Offspring
Commentary: Preimplantation Genetic Diagnosis
Article was published in

Clinical Oncology

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2009 Issue Supplementum
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