Who should do genetic counseling, and under what circumstances?

Interstitial deletions of chromosome 6q: genotype-phenotype correlation utilizing array CGH.

Clinical genetics·2007

The cerebellar transcriptome during postnatal development of the Ts1Cje mouse, a segmental trisomy model for Down syndrome.

Human molecular genetics·2004

Effects of genetic background on cardiovascular anomalies in the Ts16 mouse.

Developmental dynamics : an official publication of the American Association of Anatomists·2004

Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes.

Developmental dynamics : an official publication of the American Association of Anatomists·2004

Role of mitochondrial superoxide dismutase in contraction-induced generation of reactive oxygen species in skeletal muscle extracellular space.

American journal of physiology. Cell physiology·2004

Genetic modification of prenatal lethality and dilated cardiomyopathy in Mn superoxide dismutase mutant mice.

Free radical biology & medicine·2001

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

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

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Who should do genetic counseling, and under what circumstances?

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Interstitial deletions of chromosome 6q: genotype-phenotype correlation utilizing array CGH.

The cerebellar transcriptome during postnatal development of the Ts1Cje mouse, a segmental trisomy model for Down syndrome.

Effects of genetic background on cardiovascular anomalies in the Ts16 mouse.

Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes.

Role of mitochondrial superoxide dismutase in contraction-induced generation of reactive oxygen species in skeletal muscle extracellular space.

Genetic modification of prenatal lethality and dilated cardiomyopathy in Mn superoxide dismutase mutant mice.

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Multisite neural tube closure in humans.

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.

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Who should do genetic counseling, and under what circumstances?

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