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UnknownNo Association of Early-Onset Breast or Ovarian Cancer with Early-Onset Cancer in Relatives in <i>BRCA1</i> or <i>BRCA2</i> Mutation Families.
Not available
S-EPMC8305427 | biostudies-literature
UnknownTesticular Sertoli cell tumour and potentially testicular Leydig cell tumour are features of DICER1 syndrome.
Not available
S-EPMC9743800 | biostudies-literature
UnknownGEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Pathogenic Variant Carriers.
Not available
S-EPMC6220051 | biostudies-literature
UnknownThe plasma protein fibrinogen stabilizes clusters of red blood cells in microcapillary flows.
Not available
S-EPMC3949293 | biostudies-literature
UnknownConstitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants.
Not available
S-EPMC11126593 | biostudies-literature
TranscriptomicsKFAM CGH
Breast cancer samples from patients with BRCA2 mutation. Comparative genomic hybridization by array of BRCA2 tumors.
ORGANISM(S): Homo sapiens 
2012-11-23 | E-MEXP-3690 | biostudies-arrayexpress
UnknownGermline copy number variation of genes involved in chromatin remodelling in families suggestive of Li-Fraumeni syndrome with brain tumours.
Not available
S-EPMC3831081 | biostudies-literature
UnknownThe <i>FANCM</i>:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer.
Not available
S-EPMC6825205 | biostudies-literature
UnknownPsychological and ethical issues raised by genomic in paediatric care pathway, a qualitative analysis with parents and childhood cancer patients.
Not available
S-EPMC11577070 | biostudies-literature
UnknownThe "extreme phenotype approach" applied to male breast cancer allows the identification of rare variants of ATR as potential breast cancer susceptibility alleles.
Not available
S-EPMC9904323 | biostudies-literature
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