A-Z Patient information leaflets and videos

A

• ATM gene

B

• BAP1 Tumour Predisposition Syndrome
• Bowel Polyps or Young Onset Bowel or Endometrial Cancer - Genetic Testing for Inherited Causes (R211)
• BRCA1
• BRCA1, BRCA2 and PALB2 (Breast-, Ovarian-, Prostate- and Pancreatic cancers) (R444.1)
• BRCA2
• Breast and Ovarian cancer - RAD51C gene
• Breast and Ovarian cancer - RAD51D gene
• Breast cancer - liquid biopsy testing
• BRIP1

C

• Cancer and genetics - patient information leaflet
• Cancer - Diagnostic genetic testing for inherited causes
• CHEK2 gene
• Circulating Tumour (ct) DNA testing - What is a ctDNA test?

D

• DICER1 Syndrome

G

• Gastro Intestinal Stromal Tumours (GIST) - Genetic Testing for Inherited Causes (R363)
• Glucokinase hyperglycaemia

L

• Li-Fraumeni Syndrome (LFS)
• Lung cancer
• Lynch Syndrome - aspirin and LS, FAQs for patients
• Lynch Syndrome (endometrial and colorectal cancers)

M

• Melanoma - Genetic Testing for Inherited Causes (R254)
• MUTYH Associated Polyposis Syndrome (MAP)

N

• Neurofibromatosis type 1 (NF1)

O

• Ovarian and Breast cancer - Genetic testing for inherited causes (R208)
• Ovarian cancer - Genetic testing for inherited causes (R207)

P

• PALB2
• Pancreatic cancer gene testing (R367)
• Pancreatitis gene testing (R175)
• Pancreatitis - Your CELA3B Test Result
• Pancreatitis - Your CFTR Test Result
• Pancreatitis - Your PRSS1 Test Result
• Pancreatitis - Your SPINK1 Test Result
• Paraganglioma and Phaeochromocytoma - Genetic testing for inherited causes (R223)
• Prenatal testing
• Prostate Cancer and Genetics
• Prostate cancer - BRCA1 and BRCA2 gene tests (R444.2)
• Prostate Cancer - Genetic Testing for Inherited Causes (R430)
• PTEN Hamartoma Tumour Syndrome - Patient information

R

• Rare chromosome and gene disorder guides
• Rare Disease - Seeking a Rare Disease Diagnosis
• Renal - HLRCC: Hereditary Leiomyomatosis and Renal Cell Cancer
• Renal - MET and Hereditary Papillary Renal Cell Cancer (HPRC)

S

• Sickle Cell

W

• Whole Genome Sequencing