A familial translocation t(6q+;8q-) identified by fluorescence microscopy

Novel mutation of the initiation codon of PAX9 causes oligodontia.

Journal of dental research·2004

BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age.

Journal of medical genetics·2001

Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man.

Journal of medical genetics·2000

Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNA.

Genomics·1999

Studies of the cranial base in 23 patients with cri-du-chat syndrome suggest a cranial developmental field involved in the condition.

American journal of medical genetics·1999

CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24.

Human molecular genetics·1997

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Humangenetik·1975

Climate associated variations in the human serum albumin level.

Humangenetik·1975

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Humangenetik·1975

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Humangenetik·1975

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Humangenetik·1975

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Humangenetik·1975

Differential contributions of β-tubulin isotypes to acentrosomal oocyte meiosis in C. elegans.

The Journal of cell biology·2026

Navigating nuclear space: How Rad51 filaments promote long-range homology search during homologous recombination - Lessons from budding yeast.

DNA repair·2026

Broken chromosomes don't stay home: Tunneling nanotubes carry damaged DNA between human cells.

Molecular cell·2026

Human acrocentric chromosome short-arm de novo mutation and recombination.

Cell·2026

Ophthalmic Manifestations of KIF11-Associated Microcephaly With or Without Chorioretinopathy, Lymphedema, or Intellectual Disability: A Case Report of a Novel Variant.

The American journal of case reports·2026

MAGIC populations: a next-generation framework for dissecting complex quantitative traits and accelerating molecular breeding in crops.

Frontiers in plant science·2026

Related Experiment Videos

A familial translocation t(6q+;8q-) identified by fluorescence microscopy

Related Concept Videos

Novel mutation of the initiation codon of PAX9 causes oligodontia.

BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age.

Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man.

Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNA.

Studies of the cranial base in 23 patients with cri-du-chat syndrome suggest a cranial developmental field involved in the condition.

CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24.

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Climate associated variations in the human serum albumin level.

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Differential contributions of β-tubulin isotypes to acentrosomal oocyte meiosis in C. elegans.

Navigating nuclear space: How Rad51 filaments promote long-range homology search during homologous recombination - Lessons from budding yeast.

Broken chromosomes don't stay home: Tunneling nanotubes carry damaged DNA between human cells.

Human acrocentric chromosome short-arm de novo mutation and recombination.

Ophthalmic Manifestations of KIF11-Associated Microcephaly With or Without Chorioretinopathy, Lymphedema, or Intellectual Disability: A Case Report of a Novel Variant.

MAGIC populations: a next-generation framework for dissecting complex quantitative traits and accelerating molecular breeding in crops.

Related Experiment Videos

A familial translocation t(6q+;8q-) identified by fluorescence microscopy

Related Concept Videos

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