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Molekulargenetische Diagnostik

Moleculargenetic Diagnostics

Contact person for molecular genetics tests

Frau Birgit Neitzel
Tel. +49 (0)89/30 90 886-553

Moleculargenetic Diagnostics

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Hereditary tumour diseases, gastroenterology

Prof. Dr. med. Elke Holinski-Feder, Brigitte Schönfeld, Ärztin, Dr. rer. nat. Andreas Laner

Adenomatous Polyposis coli, FAP - APC

Adenomatous Polyposis coli, MAP - MUTYH

Birt-Hogg-Dubé Syndrome - FLCN

Breast and Ovarial Carcinoma - BRCA1, BRCA2, ATM, CHEK2, RAD51C

Carney Complex - PRKAR1A

Constitutive MMR-defiziency (CMMR-D) syndrome

Cowden Syndrome - PTEN

Gastric Cancer, Diffuse - CDH1

Gorlin Syndrome - PTCH1

HNPCC - MLH1, MSH2, MSH6, PMS2

Juvenile Polyposis coli - BMPR1A, SMAD4, ENG

Leiomyomatosis, HLRCC - FH

Li-Fraumeni Syndrome - p53

Malignant Melanoma - CDKN2A (p16)

Microsatellite analysis from tumor tissue

Morbus Crohn - CARD15

Morbus Osler - ENG, ACVRL1

Multiple Endocrine Neoplasia Type 1, MEN 1 - MEN1

Multiple Endocrine Neoplasia Type 2A, MEN 2A - RET

Multiple Endocrine Neoplasia Type 2B, MEN2B - RET

Pancreas Carcinoma, FPC - PALB2, p16

Pankreatitis - PRSS1, SPINK1, CFTR

Paragangliom-Pheochromocytoma Syndrome Typ PGL1, PGL4 - SDHB, SDHD

Peutz-Jeghers Syndrome - STK11

Schwannomatosis - SMARCB1

Von-Hippel-Lindau Syndrome - VHL

Wilms Tumor, Nephroblastoma - WT1

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