A child with interstitial deletion of chromosome No. 5

Targeted sequencing of BRCA1 and BRCA2 across a large unselected breast cancer cohort suggests that one-third of mutations are somatic.

Annals of oncology : official journal of the European Society for Medical Oncology·2016

Familial aggregation of stroke amongst young patients in Lund Stroke Register.

European journal of neurology·2015

Health needs assessment for medical genetic services for congenital disorders in middle- and low-income nations.

Journal of community genetics·2013

Are 25 SNPs from the CARDIoGRAM study associated with ischaemic stroke?

European journal of neurology·2013

Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study.

British journal of cancer·2012

Genetic screening in Europe.

Public health genomics·2010

Targeting RASL12 by miR-6791-5p fuels malignant progression in lung adenocarcinoma.

Hereditas·2026

Haplotype-based validation of genomic regions for breeding of new Nordic apples.

Hereditas·2026

miR-335-3p acts as a tumor suppressor in esophageal squamous cell carcinoma and predicts favorable prognosis.

Hereditas·2026

SNP rs7430456 mediated LINC00578 drives triple negative breast cancer through regulating miR-143-5p expression.

Hereditas·2026

BFLF1 gene polymorphisms are associated with increased mortality in patients with EBV-associated diseases.

Hereditas·2026

miR-1-3p, as a novel diagnostic and prognostic biomarker, aggravates pancreatic acinar cell injury in acute pancreatitis by targeting GNPTAB.

Hereditas·2026

Pediatric Varicocele as the Presenting Sign of Nutcracker Syndrome: An Ultrasound Case Report.

International medical case reports journal·2026

Early postoperative red cell distribution width is associated with prolonged hospital stay and complications after non-cardiac surgery in neonates.

International journal of medical sciences·2026

Successful Management of a Neonate With Tricuspid Atresia, Double Outlet Right Ventricle, and L-malposed Great Arteries.

Cureus·2026

Related Experiment Videos

A child with interstitial deletion of chromosome No. 5

Related Concept Videos

Targeted sequencing of BRCA1 and BRCA2 across a large unselected breast cancer cohort suggests that one-third of mutations are somatic.

Familial aggregation of stroke amongst young patients in Lund Stroke Register.

Health needs assessment for medical genetic services for congenital disorders in middle- and low-income nations.

Are 25 SNPs from the CARDIoGRAM study associated with ischaemic stroke?

Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study.

Genetic screening in Europe.

Targeting RASL12 by miR-6791-5p fuels malignant progression in lung adenocarcinoma.

Haplotype-based validation of genomic regions for breeding of new Nordic apples.

miR-335-3p acts as a tumor suppressor in esophageal squamous cell carcinoma and predicts favorable prognosis.

SNP rs7430456 mediated LINC00578 drives triple negative breast cancer through regulating miR-143-5p expression.

BFLF1 gene polymorphisms are associated with increased mortality in patients with EBV-associated diseases.

miR-1-3p, as a novel diagnostic and prognostic biomarker, aggravates pancreatic acinar cell injury in acute pancreatitis by targeting GNPTAB.

Pediatric Varicocele as the Presenting Sign of Nutcracker Syndrome: An Ultrasound Case Report.

Early postoperative red cell distribution width is associated with prolonged hospital stay and complications after non-cardiac surgery in neonates.

Successful Management of a Neonate With Tricuspid Atresia, Double Outlet Right Ventricle, and L-malposed Great Arteries.

Related Experiment Videos

A child with interstitial deletion of chromosome No. 5

Related Concept Videos

Related Articles