Fluorescent chromosome polymorphisms: frequencies and segregations in a Dutch population

Evaluation of exclusion prenatal and exclusion preimplantation genetic diagnosis for Huntington's disease in the Netherlands.

Clinical genetics·2012

Parent-of-origin specific linkage and association of the IGF2 gene region with birth weight and adult metabolic risk factors.

International journal of obesity (2005)·2009

Common SNPs in LEP and LEPR associated with birth weight and type 2 diabetes-related metabolic risk factors in twins.

International journal of obesity (2005)·2008

Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification.

Clinical genetics·2007

The PIP5K2A and RGS4 genes are differentially associated with deficit and non-deficit schizophrenia.

Genes, brain, and behavior·2007

Historical development of analysing large-scale changes in the human genome.

Cytogenetic and genome research·2006

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

Surviving Males With PORCN Variants: Expanding the Clinical, Molecular, and Mechanistic Spectrum.

Clinical genetics·2026

A De Novo DHX16 Variant Associated With Neuromuscular Oculoauditory Syndrome Regulates Pre-mRNA Splicing In Vitro.

Clinical genetics·2026

Clinical and Genetic Profile of One Molecularly Confirmed and One Clinically Suspected Case of LZTR1-Related Noonan Syndrome.

Clinical genetics·2026

A homozygous lamin B receptor variant resulting in Pelger-Huët anomaly without skeletal dysplasia.

Nucleus (Austin, Tex.)·2026

ZATELLITE: a toolkit to visualize and manipulate human centromeres in live cells using synthetic zinc fingers.

bioRxiv : the preprint server for biology·2026

Recurrent Single-Nucleotide Insertions in the Mitochondrial Second Light-Strand Promoter Cause Tubulointerstitial Kidney Disease.

medRxiv : the preprint server for health sciences·2026

Structural determination of human nucleosomes reconstituted by the ExACT platform.

bioRxiv : the preprint server for biology·2026

The linker histone H1.4 condenses chromatin in maturing postmitotic neurons.

bioRxiv : the preprint server for biology·2026

dif-XerCD is Required for Chromosome Segregation During cSDR-Dependent Growth in Escherichia coli.

Molecular and cellular biology·2026

Related Experiment Videos

Fluorescent chromosome polymorphisms: frequencies and segregations in a Dutch population

Related Concept Videos

Evaluation of exclusion prenatal and exclusion preimplantation genetic diagnosis for Huntington's disease in the Netherlands.

Parent-of-origin specific linkage and association of the IGF2 gene region with birth weight and adult metabolic risk factors.

Common SNPs in LEP and LEPR associated with birth weight and type 2 diabetes-related metabolic risk factors in twins.

Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification.

The PIP5K2A and RGS4 genes are differentially associated with deficit and non-deficit schizophrenia.

Historical development of analysing large-scale changes in the human genome.

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.

Surviving Males With PORCN Variants: Expanding the Clinical, Molecular, and Mechanistic Spectrum.

A De Novo DHX16 Variant Associated With Neuromuscular Oculoauditory Syndrome Regulates Pre-mRNA Splicing In Vitro.

Clinical and Genetic Profile of One Molecularly Confirmed and One Clinically Suspected Case of LZTR1-Related Noonan Syndrome.

A homozygous lamin B receptor variant resulting in Pelger-Huët anomaly without skeletal dysplasia.

ZATELLITE: a toolkit to visualize and manipulate human centromeres in live cells using synthetic zinc fingers.

Recurrent Single-Nucleotide Insertions in the Mitochondrial Second Light-Strand Promoter Cause Tubulointerstitial Kidney Disease.

Structural determination of human nucleosomes reconstituted by the ExACT platform.

The linker histone H1.4 condenses chromatin in maturing postmitotic neurons.

dif-XerCD is Required for Chromosome Segregation During cSDR-Dependent Growth in Escherichia coli.

Related Experiment Videos

Fluorescent chromosome polymorphisms: frequencies and segregations in a Dutch population

Related Concept Videos

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