Cytogenetic aspects of human male meiosis

Self-assessed remission rates after electroconvulsive therapy of depressive disorders.

European psychiatry : the journal of the Association of European Psychiatrists·2017

Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome).

Journal of medical genetics·2007

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.

Human mutation·2004

[Santiago Ramon y Cajal and neurobiology].

Svensk medicinhistorisk tidskrift·2002

MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region.

Brain & development·2001

Guidelines for reporting clinical features in cases with MECP2 mutations.

Brain & development·2001

Genetic aspects of immunoglobulin A deficiency.

Advances in human genetics·1990

Structural defects in inherited and giant platelet disorders.

Advances in human genetics·1990

The Meiotic Spindle, Mechanisms of Chromosome Segregation and Aneuploidy in Aging Human Oocytes: An Update Review.

Medicina (Kaunas, Lithuania)·2026

Application of Whole-Exome Sequencing in Identifying the Molecular Basis of Idiopathic Male Infertility.

Journal of clinical medicine·2026

A CDC20 allelic series reveals stage-specific control of metaphase-to-anaphase transitions during mitosis and meiosis in rice.

Science China. Life sciences·2026

Lamin B1 Coordinates the Assembly of the Nuclear Lamina.

Journal of cell science·2026

Machine-Readable Database for Genotype-Phenotype Analyses in Rare Diseases Using FKTN-related Congenital Muscular Dystrophies as a Prototype.

Research square·2026

NEMP1 organizes the meiotic telomere LINC interface to control chromosome movement and telomere integrity.

bioRxiv : the preprint server for biology·2026

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Cytogenetic aspects of human male meiosis

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Self-assessed remission rates after electroconvulsive therapy of depressive disorders.

Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome).

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.

[Santiago Ramon y Cajal and neurobiology].

MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region.

Guidelines for reporting clinical features in cases with MECP2 mutations.

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Application of Whole-Exome Sequencing in Identifying the Molecular Basis of Idiopathic Male Infertility.

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Cytogenetic aspects of human male meiosis

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