Genetic counseling: meeting today's and tomorrow's needs

Loss of heterozygosity on the long arm of human chromosome 7 in sporadic renal cell carcinomas.

Oncogene·1997

Mutations in the arginine-rich protein gene (ARP) in pancreatic cancer.

Oncogene·1997

Frequent breakpoints in the region surrounding FRA3B in sporadic renal cell carcinomas.

Oncogene·1997

Mutations in the arginine-rich protein gene, in lung, breast, and prostate cancers, and in squamous cell carcinoma of the head and neck.

Cancer research·1996

A gene from human chromosomal band 3p21.1 encodes a highly conserved arginine-rich protein and is mutated in renal cell carcinomas.

Oncogene·1996

Isolation of two contigs of overlapping cosmids derived from human chromosomal band 3p21.1 and identification of 5 new 3p21.1 genes.

Somatic cell and molecular genetics·1994

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

Prenatal environmental determinants of aromatase brain-promoter methylation in cord blood: chemical, airborne, pharmacological, and nutritional factors.

Environmental epigenetics·2026

Proximity-ligation metagenomics reveals differential plasmid and chromosomal antimicrobial resistance gene carriage in disrupted gut ecosystems.

iScience·2026

Intrinsic anti-tumorigenic properties of the skin epithelium promote cancer resistance in naked mole-rats.

iScience·2026

DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans.

iScience·2026

DNA methylation profiling identifies long-range epigenetic silencing of clustered protocadherins as a key determinant of meningioma progression.

Nature communications·2026

Integrative Analysis of Nucleotide Metabolism-Related Genes Reveals a Diagnostic Signature and In Silico Functional Disruption in Hypertrophic Scarring.

Journal of burn care & research : official publication of the American Burn Association·2026

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Genetic counseling: meeting today's and tomorrow's needs

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Loss of heterozygosity on the long arm of human chromosome 7 in sporadic renal cell carcinomas.

Mutations in the arginine-rich protein gene (ARP) in pancreatic cancer.

Frequent breakpoints in the region surrounding FRA3B in sporadic renal cell carcinomas.

Mutations in the arginine-rich protein gene, in lung, breast, and prostate cancers, and in squamous cell carcinoma of the head and neck.

A gene from human chromosomal band 3p21.1 encodes a highly conserved arginine-rich protein and is mutated in renal cell carcinomas.

Isolation of two contigs of overlapping cosmids derived from human chromosomal band 3p21.1 and identification of 5 new 3p21.1 genes.

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Multisite neural tube closure in humans.

Prenatal environmental determinants of aromatase brain-promoter methylation in cord blood: chemical, airborne, pharmacological, and nutritional factors.

Proximity-ligation metagenomics reveals differential plasmid and chromosomal antimicrobial resistance gene carriage in disrupted gut ecosystems.

Intrinsic anti-tumorigenic properties of the skin epithelium promote cancer resistance in naked mole-rats.

DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans.

DNA methylation profiling identifies long-range epigenetic silencing of clustered protocadherins as a key determinant of meningioma progression.

Integrative Analysis of Nucleotide Metabolism-Related Genes Reveals a Diagnostic Signature and In Silico Functional Disruption in Hypertrophic Scarring.

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Genetic counseling: meeting today's and tomorrow's needs

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