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Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation

Human molecular genetics, 1999-11, Vol.8 (12), p.2293-2302

1999

Volltextzugriff (PDF)

Guidelines for the diagnosis of fragile X syndrome

Journal of medical genetics, 1993, Vol.30 (5), p.410-413

1993

Volltextzugriff (PDF)

Hypomethylation of an Expanded FMR1 Allele Is Not Associated with a Global DNA Methylation Defect

American journal of human genetics, 1999-11, Vol.65 (5), p.1375-1386

1999

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The giemsa banding pattern of canine chromosomes, using a cell synchronization technique

Genome, 1991-06, Vol.34 (3), p.407

1991

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Heritable fragile sites on human chromosomes. XI: factors affecting expression of fragile sites at 10q25, 16q22, and 17p12

American journal of human genetics, 1984, Vol.36 (1), p.110-122

1984

Volltextzugriff (PDF)

Chromosomal fragile site expression in dogs. I, Breed specific differences

American journal of medical genetics, 1991-08, Vol.40 (2), p.214-222

1991

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Chromosomal fragile site expression in dogs. II, Expression in boxer dogs with mast cell tumors

American journal of medical genetics, 1991-08, Vol.40 (2), p.223-229

1991

Volltextzugriff (PDF)

A novel Robertsonian translocation in a family of Walker hounds

Genome, 1991-08, Vol.34 (4), p.677

1991

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Expression in fibroblast culture of the satellited-X chromosome associated with familial sex-linked mental retardation

Human genetics, 1980-02, Vol.53 (2), p.267-269

1980

Volltextzugriff (PDF)

Thymidylate synthetase inhibitors and fragile site expression in lymphocytes

American journal of human genetics, 1983-11, Vol.35 (6), p.1276-1283

1983

Volltextzugriff (PDF)

CFU-S in individual erythroid colonies derived in vitro from adult mouse marrow

Nature (London), 1979-06, Vol.279 (5715), p.718-720

1979

Volltextzugriff (PDF)

Heritable fragile sites on human chromosomes. X. New folate-sensitive fragile sites: 6p23, 9p21, 9q32, and 11q23

American journal of human genetics, 1983-05, Vol.35 (3), p.432-437

1983

Volltextzugriff (PDF)

FMC-HU-1-B: A lymphoma B-cell line with unusual characteristics

Leukemia research, 1985, Vol.9 (1), p.97-111

1985

Volltextzugriff (PDF)

Guidelines for the Preparation and Analysis of the Fragile X Chromosome in Lymphocytes

American journal of medical genetics, 1991-02, Vol.38 (2-3), p.400-403

1991

Volltextzugriff (PDF)

Fragile Sites in Chromosomes: Possible Model for the Study of Spontaneous Chromosome Breakage

Science (American Association for the Advancement of Science), 1983-04, Vol.220 (4592), p.69-70

1983

Volltextzugriff (PDF)

Fragile X chromosome and chromosome condensation

Annales de génétique, 1983, Vol.26 (3), p.171

1983

Volltextzugriff (PDF)

The fragile X chromosome: Current methods

American journal of medical genetics, 1982-04, Vol.11 (4), p.489-495

1982

Volltextzugriff (PDF)

Fully Expanded FMR1CGG Repeats Exhibit a Length-and Differentiation-Dependent Instability in Cell Hybrids That is Independent of DNA Methylation

Human molecular genetics, 1999-11, Vol.8 (12), p.2293-2302

1999

Volltextzugriff (PDF)

Section E6 of the ACMG technical standards and guidelines: chromosome studies for acquired abnormalities

Genetics in medicine, 2005-09, Vol.7 (7), p.509-513

2005

Volltextzugriff (PDF)

Interferon-inducible fragile site on chromosome 16

The Lancet (British edition), 1981-01, Vol.1 (8211), p.108-108

1981

Volltextzugriff (PDF)

Clinical outcomes of four patients with microdeletion in the long arm of chromosome 2

American journal of medical genetics, 1998-06, Vol.78 (1), p.36-43

1998

Volltextzugriff (PDF)

Cytogenetic evaluation of four canine mast cell tumors

Cancer genetics and cytogenetics, 1991-05, Vol.53 (1), p.105-112

1991

Volltextzugriff (PDF)

Guidelines for the diagnosis of fragile X syndrome. National Fragile X Foundation

Journal of medical genetics, 1993-05, Vol.30 (5), p.410-413

1993

Volltextzugriff (PDF)

Fragile sites in chromosomes: Possible model for the study of spontaneous chromosomes breakage

Science (American Association for the Advancement of Science), 1983-01, Vol.220 (4592), p.69-71

1983

Volltextzugriff (PDF)

FMC-Hu-1-B: A lymphoma B-cell line with unusual characteristics

Leukemia research, 1984-01, Vol.9 (1), p.97-111

1984

Volltextzugriff (PDF)

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Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation

Guidelines for the diagnosis of fragile X syndrome

Hypomethylation of an Expanded FMR1 Allele Is Not Associated with a Global DNA Methylation Defect

The giemsa banding pattern of canine chromosomes, using a cell synchronization technique

Heritable fragile sites on human chromosomes. XI: factors affecting expression of fragile sites at 10q25, 16q22, and 17p12

Chromosomal fragile site expression in dogs. I, Breed specific differences

Chromosomal fragile site expression in dogs. II, Expression in boxer dogs with mast cell tumors

A novel Robertsonian translocation in a family of Walker hounds

Expression in fibroblast culture of the satellited-X chromosome associated with familial sex-linked mental retardation

Thymidylate synthetase inhibitors and fragile site expression in lymphocytes

CFU-S in individual erythroid colonies derived in vitro from adult mouse marrow

Heritable fragile sites on human chromosomes. X. New folate-sensitive fragile sites: 6p23, 9p21, 9q32, and 11q23

FMC-HU-1-B: A lymphoma B-cell line with unusual characteristics

Guidelines for the Preparation and Analysis of the Fragile X Chromosome in Lymphocytes

Fragile Sites in Chromosomes: Possible Model for the Study of Spontaneous Chromosome Breakage

Fragile X chromosome and chromosome condensation

The fragile X chromosome: Current methods

Fully Expanded FMR1CGG Repeats Exhibit a Length-and Differentiation-Dependent Instability in Cell Hybrids That is Independent of DNA Methylation

Section E6 of the ACMG technical standards and guidelines: chromosome studies for acquired abnormalities

Interferon-inducible fragile site on chromosome 16

Clinical outcomes of four patients with microdeletion in the long arm of chromosome 2

Cytogenetic evaluation of four canine mast cell tumors

Guidelines for the diagnosis of fragile X syndrome. National Fragile X Foundation

Fragile sites in chromosomes: Possible model for the study of spontaneous chromosomes breakage

FMC-Hu-1-B: A lymphoma B-cell line with unusual characteristics

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