Parental age, and how extra isochromosomes (secondary trisomy) arise

Monosomal karyotype in myelodysplastic syndromes, with or without monosomy 7 or 5, is prognostically worse than an otherwise complex karyotype.

Leukemia·2010

Refined cytogenetic-risk categorization for overall and leukemia-free survival in primary myelofibrosis: a single center study of 433 patients.

Leukemia·2010

Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study.

Journal of medical genetics·2006

Deletion of 2q37 and duplication of 10q24: two cases in the same family and review of the literature.

Annales de genetique·2001

Cytogenetic analysis and construction of a BAC contig across a common neocentromeric region from 9p.

Chromosoma·2001

Prenatal diagnosis of 22q11.2 deletion when ultrasound examination reveals a heart defect.

Genetics in medicine : official journal of the American College of Medical Genetics·2001

Rare Novel Genetic Variants of the OFD1 Gene Associated With a Familial Form and a Sporadic Case of Long Bone Atypical Fractures.

Clinical genetics·2026

Genetics in Heterotaxy: A Case Series and Literature Review on DNAH9, PKD1L1, MMP21, and GDF1.

Clinical genetics·2026

The First Case of Isolated Uterine Atony as the Only Symptom in an Individual With ACTG2-Associated Visceral Myopathy.

Clinical genetics·2026

Sotos and Malan Syndromes in Childhood: Molecular and Clinical Findings From a Nationwide Cohort of 48 Patients.

Clinical genetics·2026

Genetic Architecture of Pediatric Cardiomyopathies Assessed by Whole-Exome Sequencing: Insights Into Early-Onset and Syndromic Forms.

Clinical genetics·2026

Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.

Clinical genetics·2026

Reduced dosage of Kmt2d modifies Tbx1 haploinsufficiency toward phenotypes of 22q11.2DS.

JCI insight·2026

Exploring the Causal Relationship Between Sex Hormones and Depression by Means of Two-Sample Mendelian Randomization Analysis.

Actas espanolas de psiquiatria·2026

Generation of 5 induced pluripotent stem cell lines with copy number variations in 22q11.2.

Stem cell research·2026

Whole-transcriptome profiling of the fat body identifies aae-miR-283-ApoLp-Ⅱ/Ⅰ regulation associated with lipid transport and ovarian development in Aedes aegypti.

Insect biochemistry and molecular biology·2026

Androgen signaling via sympathetic neurons regulates allergic pulmonary inflammation.

Science immunology·2026

VDR BsmI polymorphism and obesity in vitamin D deficiency among undergraduate students: a cross-sectional study.

Molecular biology reports·2026

Related Experiment Videos

Parental age, and how extra isochromosomes (secondary trisomy) arise

Related Concept Videos

Monosomal karyotype in myelodysplastic syndromes, with or without monosomy 7 or 5, is prognostically worse than an otherwise complex karyotype.

Refined cytogenetic-risk categorization for overall and leukemia-free survival in primary myelofibrosis: a single center study of 433 patients.

Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study.

Deletion of 2q37 and duplication of 10q24: two cases in the same family and review of the literature.

Cytogenetic analysis and construction of a BAC contig across a common neocentromeric region from 9p.

Prenatal diagnosis of 22q11.2 deletion when ultrasound examination reveals a heart defect.

Rare Novel Genetic Variants of the OFD1 Gene Associated With a Familial Form and a Sporadic Case of Long Bone Atypical Fractures.

Genetics in Heterotaxy: A Case Series and Literature Review on DNAH9, PKD1L1, MMP21, and GDF1.

The First Case of Isolated Uterine Atony as the Only Symptom in an Individual With ACTG2-Associated Visceral Myopathy.

Sotos and Malan Syndromes in Childhood: Molecular and Clinical Findings From a Nationwide Cohort of 48 Patients.

Genetic Architecture of Pediatric Cardiomyopathies Assessed by Whole-Exome Sequencing: Insights Into Early-Onset and Syndromic Forms.

Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.

Reduced dosage of Kmt2d modifies Tbx1 haploinsufficiency toward phenotypes of 22q11.2DS.

Exploring the Causal Relationship Between Sex Hormones and Depression by Means of Two-Sample Mendelian Randomization Analysis.

Generation of 5 induced pluripotent stem cell lines with copy number variations in 22q11.2.

Whole-transcriptome profiling of the fat body identifies aae-miR-283-ApoLp-Ⅱ/Ⅰ regulation associated with lipid transport and ovarian development in Aedes aegypti.

Androgen signaling via sympathetic neurons regulates allergic pulmonary inflammation.

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Parental age, and how extra isochromosomes (secondary trisomy) arise

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