The Colton blood groups in monosomy 7 of the bone marrow

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

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Birth defects original article series·1996

Multisite neural tube closure in humans.

Birth defects original article series·1996

Adolescent Survival in Thoracoabdominal Ectopia Cordis With Complex Single Ventricle Physiology and Complete Atrioventricular Block.

JACC. Case reports·2026

Physeal stress injury and osteochondrosis in the ankle and foot of young athletes.

British medical bulletin·2026

Outcomes of Growth Modulation for Residual Clubfoot Deformities.

Foot & ankle specialist·2026

[Clinical analysis of spinal muscular atrophy complicated with hypoglycemia in 5 children].

Zhonghua er ke za zhi = Chinese journal of pediatrics·2026

Oropharyngeal Gonorrhea and Chlamydia Testing in the Pediatric Emergency Department.

Clinical pediatrics·2026

Parental monitoring and therapeutic adherence in adolescents and young adults with type 1 diabetes mellitus: Systematic review with meta-analysis.

Diabetic medicine : a journal of the British Diabetic Association·2026

Related Experiment Videos

The Colton blood groups in monosomy 7 of the bone marrow

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.

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Multisite neural tube closure in humans.

Adolescent Survival in Thoracoabdominal Ectopia Cordis With Complex Single Ventricle Physiology and Complete Atrioventricular Block.

Physeal stress injury and osteochondrosis in the ankle and foot of young athletes.

Outcomes of Growth Modulation for Residual Clubfoot Deformities.

[Clinical analysis of spinal muscular atrophy complicated with hypoglycemia in 5 children].

Oropharyngeal Gonorrhea and Chlamydia Testing in the Pediatric Emergency Department.

Parental monitoring and therapeutic adherence in adolescents and young adults with type 1 diabetes mellitus: Systematic review with meta-analysis.

Related Experiment Videos

The Colton blood groups in monosomy 7 of the bone marrow

Related Concept Videos

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