The MNSs blood groups of families with chromosome 4 rearrangements

The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.

Leukemia·2017

Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemia.

Leukemia·2016

MicroRNA-related sequence variations in human cancers.

Human genetics·2013

Recurrent and founder mutations in the PMS2 gene.

Clinical genetics·2012

Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene.

Clinical genetics·2011

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease.

Gut·2010

Evidence for Reduced Somatic T-Cell Receptor Sequence Diversity Profiles Among Midwestern Amish in an Aging Cohort Study.

Annals of human genetics·2026

MYLK c.4079G>A, p.(Gly1360Asp) Variant Associated With Hereditary Thoracic Aortic Diseases and Early Onset Aortic Dissection.

Annals of human genetics·2026

Exome Sequencing Identifies Novel Variants Causing Hearing Loss in Three Consanguineous Pakistani Families: Insights From Genomics and Bioinformatics Analyses.

Annals of human genetics·2026

What Uniparental Lineages Tell Us About the Prehistoric Human Colonization of the Americas.

Annals of human genetics·2026

Genomic Structural Equation Modeling Identifies a Shared Inflammatory Genetic Dimension Across Inflammatory Arthritis Phenotypes and Biomarkers.

Annals of human genetics·2026

Genetically Proxied Leukocyte Telomere Length and Epigenetic Age Acceleration in Relation to Healthspan: A Mendelian Randomization Study.

Annals of human genetics·2026

Successful management of high-risk proliferative diabetic retinopathy during pregnancy with intravitreal faricimab.

Oxford medical case reports·2026

Twin pregnancies conceived by assisted reproductive treatments and the risk of long-term offspring pediatric neurological morbidity.

European journal of obstetrics, gynecology, and reproductive biology·2026

Periconceptional and early-pregnancy exposure to SGLT2 inhibitors and congenital malformations: a systematic review and meta-analysis.

Endocrine·2026

Not all Day-4 embryos are equal: developmental stage predicts outcomes after single embryo transfer.

Journal of assisted reproduction and genetics·2026

RAC1-YAP1-PIEZO1 signaling axis links intrauterine inflammation to uterine hypercontractility and preterm labor.

Biology of reproduction·2026

Prenatal Diagnosis of FLNA-related Cerebral Periventricular Nodular Heterotopia Presented with Enlarged Cisterna Magna Identified in the Second Trimester: Two Case Reports.

Journal of medical ultrasound·2026

Related Experiment Videos

The MNSs blood groups of families with chromosome 4 rearrangements

Related Concept Videos

The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.

Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemia.

MicroRNA-related sequence variations in human cancers.

Recurrent and founder mutations in the PMS2 gene.

Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene.

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease.

Evidence for Reduced Somatic T-Cell Receptor Sequence Diversity Profiles Among Midwestern Amish in an Aging Cohort Study.

MYLK c.4079G>A, p.(Gly1360Asp) Variant Associated With Hereditary Thoracic Aortic Diseases and Early Onset Aortic Dissection.

Exome Sequencing Identifies Novel Variants Causing Hearing Loss in Three Consanguineous Pakistani Families: Insights From Genomics and Bioinformatics Analyses.

What Uniparental Lineages Tell Us About the Prehistoric Human Colonization of the Americas.

Genomic Structural Equation Modeling Identifies a Shared Inflammatory Genetic Dimension Across Inflammatory Arthritis Phenotypes and Biomarkers.

Genetically Proxied Leukocyte Telomere Length and Epigenetic Age Acceleration in Relation to Healthspan: A Mendelian Randomization Study.

Successful management of high-risk proliferative diabetic retinopathy during pregnancy with intravitreal faricimab.

Twin pregnancies conceived by assisted reproductive treatments and the risk of long-term offspring pediatric neurological morbidity.

Periconceptional and early-pregnancy exposure to SGLT2 inhibitors and congenital malformations: a systematic review and meta-analysis.

Not all Day-4 embryos are equal: developmental stage predicts outcomes after single embryo transfer.

RAC1-YAP1-PIEZO1 signaling axis links intrauterine inflammation to uterine hypercontractility and preterm labor.

Prenatal Diagnosis of FLNA-related Cerebral Periventricular Nodular Heterotopia Presented with Enlarged Cisterna Magna Identified in the Second Trimester: Two Case Reports.

Related Experiment Videos

The MNSs blood groups of families with chromosome 4 rearrangements

Related Concept Videos

Related Articles