A highly informative CA/GT repeat polymorphism in intron 38 of the human neurofibromatosis type 1 (NF1) gene

ESGO-ESMO-ESP consensus conference recommendations on ovarian cancer: pathology and molecular biology and early, advanced and recurrent disease.

Annals of oncology : official journal of the European Society for Medical Oncology·2024

Molecular profiling and feasibility using a comprehensive hybrid capture panel on a consecutive series of non-small-cell lung cancer patients from a single centre.

ESMO open·2023

[Guillain-Barre syndrome and thrombocytopenia after SARS-CoV-2 vaccination with Moderna. A case report].

Revista de neurologia·2022

Genome-wide profiling of non-smoking-related lung cancer cells reveals common RB1 rearrangements associated with histopathologic transformation in EGFR-mutant tumors.

Annals of oncology : official journal of the European Society for Medical Oncology·2020

Mutational Screening of BRCA1/2 Genes as a Predictive Factor for Therapeutic Response in Epithelial Ovarian Cancer: A Consensus Guide from the Spanish Society of Pathology (SEAP-IAP) and the Spanish Society of Human Genetics (AEGH).

Virchows Archiv : an international journal of pathology·2019

Blazar spectral variability as explained by a twisted inhomogeneous jet.

Nature·2017

The impact of nationwide folic acid fortification on genetic variants associated with conotruncal heart defects.

Human genetics·2026

A genome-wide association study of cognitive impairment in a Chinese cohort of 1,040 individuals.

Human genetics·2026

Gene-based association analysis of depression risk among European ancestry Parkinson's disease patients.

Human genetics·2026

Interobserver reliability and digital morphometric characterization of constitutional chromosomal heteromorphisms in clinical cytogenetics.

Human genetics·2026

Characterization of familial short stature with or without skeletal dysplasia in a Pakistani cohort reveals founder mutations as well as novel variants.

Human genetics·2026

Geographic barrier contributed to the diversity of maternal and paternal lineages in New Guinea Island.

Human genetics·2026

Evaluating the Prognostic Significance of the H-Index and Systemic Inflammatory Parameters in IDH-Wildtype Glioblastoma Survival.

Current oncology (Toronto, Ont.)·2026

Re-Analysis on GRCh38 with the MANE Select Transcript Resolves Previously Undetected Biallelic ODAD4 Variants in Primary Ciliary Dyskinesia.

Cells·2026

The genetic landscape of RAG deficiency: Novel and founder variants in a large Algerian cohort.

Journal of human immunity·2026

Mapping Functional Transitions across Protein Homologues from a Single Simulation: Application of gEDES-HM to Adenylate Kinases.

Journal of chemical information and modeling·2026

Integrative Genetic, Transcriptomic, and Single-Cell Analyses Prioritize Druggable Candidate Genes in Knee Osteoarthritis.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology·2026

Mid-trimester sum-estimated fetal weight and gestational diabetes risk in twin pregnancies.

International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics·2026

Related Experiment Videos

A highly informative CA/GT repeat polymorphism in intron 38 of the human neurofibromatosis type 1 (NF1) gene

Related Concept Videos

ESGO-ESMO-ESP consensus conference recommendations on ovarian cancer: pathology and molecular biology and early, advanced and recurrent disease.

Molecular profiling and feasibility using a comprehensive hybrid capture panel on a consecutive series of non-small-cell lung cancer patients from a single centre.

[Guillain-Barre syndrome and thrombocytopenia after SARS-CoV-2 vaccination with Moderna. A case report].

Genome-wide profiling of non-smoking-related lung cancer cells reveals common RB1 rearrangements associated with histopathologic transformation in EGFR-mutant tumors.

Mutational Screening of BRCA1/2 Genes as a Predictive Factor for Therapeutic Response in Epithelial Ovarian Cancer: A Consensus Guide from the Spanish Society of Pathology (SEAP-IAP) and the Spanish Society of Human Genetics (AEGH).

Blazar spectral variability as explained by a twisted inhomogeneous jet.

The impact of nationwide folic acid fortification on genetic variants associated with conotruncal heart defects.

A genome-wide association study of cognitive impairment in a Chinese cohort of 1,040 individuals.

Gene-based association analysis of depression risk among European ancestry Parkinson's disease patients.

Interobserver reliability and digital morphometric characterization of constitutional chromosomal heteromorphisms in clinical cytogenetics.

Characterization of familial short stature with or without skeletal dysplasia in a Pakistani cohort reveals founder mutations as well as novel variants.

Geographic barrier contributed to the diversity of maternal and paternal lineages in New Guinea Island.

Evaluating the Prognostic Significance of the H-Index and Systemic Inflammatory Parameters in IDH-Wildtype Glioblastoma Survival.

Re-Analysis on GRCh38 with the MANE Select Transcript Resolves Previously Undetected Biallelic ODAD4 Variants in Primary Ciliary Dyskinesia.

The genetic landscape of RAG deficiency: Novel and founder variants in a large Algerian cohort.

Mapping Functional Transitions across Protein Homologues from a Single Simulation: Application of gEDES-HM to Adenylate Kinases.

Integrative Genetic, Transcriptomic, and Single-Cell Analyses Prioritize Druggable Candidate Genes in Knee Osteoarthritis.

Mid-trimester sum-estimated fetal weight and gestational diabetes risk in twin pregnancies.

Related Experiment Videos

A highly informative CA/GT repeat polymorphism in intron 38 of the human neurofibromatosis type 1 (NF1) gene

Abstract:

Related Concept Videos

Related Articles