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Guidance for Fluorescence in Situ Hybridization Testing in Hematologic Disorders

The Journal of molecular diagnostics : JMD, 2007-04, Vol.9 (2), p.134-143

2007

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Technical Standards and Guidelines for Fragile X: The First of a Series of Disease-Specific Supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics

Genetics in medicine, 2001-05, Vol.3 (3), p.200-205

2001

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Section E6.5 of the ACMG technical standards and guidelines: Chromosome studies for solid tumor abnormalities

Genetics in medicine, 2009-12, Vol.11 (12), p.890-897

2009

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16. The evolutionary conserved developmental regulome define high risk regions for long range position effects

Cancer genetics, 2018-08, Vol.224-225, p.56-56

2018

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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

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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

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50 - Systematic Mapping of Chromosomal Breakpoints in the Context of Phenotypes and Nuclear Genome Organization

Cancer genetics, 2016-06, Vol.209 (6), p.301-301

2016

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Human Factors in the Health Care Setting: A Pocket Guide for Clinical Instructors

1, 2013

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Systematic Mapping of Chromosomal Breakpoints in the Context of Phenotypes and Nuclear Genome Organization

Cancer genetics, 2016-06, Vol.209 (6), p.301-301

2016

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International Breakpoint Mapping Consortium (IBMC). Systematic Mapping of Chromosomal Breakpoints in the Context of Phenotypes and Nuclear Genome Organization

Cancer genetics, 2015-06, Vol.208 (6), p.359-360

2015

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

Genome, 1991-06, Vol.34 (3), p.407-412

1991

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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

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Section E6 of the ACMG technical standards and guidelines: Chromosome studies for acquired abnormalitie: This updated Section E6 has been incorporated into Section E: Clinical Cytogenetics of the 2005 ACMG Standards and Guidelines for Clinical Genetics Laboratories and supersedes the previous section E6

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

2005

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A novel Robertsonian translocation in a family of Walker hounds

Genome, 1991-08, Vol.34 (4), p.677-680

1991

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Guidelines for the diagnosis of fragile X syndrome

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

1993

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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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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

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Animal model: 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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INTERFERON-INDUCIBLE FRAGILE SITE ON CHROMOSOME 16

The Lancet (British edition), 1981, Vol.317 (8211), p.108-108

1981

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Title Page / Table of Contents / Abstracts of Presentations at the 31 st Annual American Cytogenetic Conference

Cytogenetic and genome research, 1993-04, Vol.63 (4), p.247-258

1993

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PRENATAL DIAGNOSIS OF FRAGILE X CHROMOSOME

The Lancet (British edition), 1982-01, Vol.319 (8263), p.99-100

1982

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FRAGILE X CHROMOSOME ASSOCIATED WITH FAMILIAL SEX-LINKED MENTAL RETARDATION: EXPRESSION IN FIBROBLAST CULTURE

JACKY, PETER BRUCE

1980

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Fragile X expression in fibroblasts

Pathology, 1983, Vol.15 (1), p.105-106

1983

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Abstracts of presentations at the Thirtieth Annual American Cytogenetics Conference

Cytogenetic and genome research, 1992-12, Vol.60 (3-4), p.257-269

1992

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

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

1985

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Guidance for Fluorescence in Situ Hybridization Testing in Hematologic Disorders

Technical Standards and Guidelines for Fragile X: The First of a Series of Disease-Specific Supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics

Section E6.5 of the ACMG technical standards and guidelines: Chromosome studies for solid tumor abnormalities

16. The evolutionary conserved developmental regulome define high risk regions for long range position effects

Fully expanded FMR1 CGG 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

50 - Systematic Mapping of Chromosomal Breakpoints in the Context of Phenotypes and Nuclear Genome Organization

Human Factors in the Health Care Setting: A Pocket Guide for Clinical Instructors

Systematic Mapping of Chromosomal Breakpoints in the Context of Phenotypes and Nuclear Genome Organization

International Breakpoint Mapping Consortium (IBMC). Systematic Mapping of Chromosomal Breakpoints in the Context of Phenotypes and Nuclear Genome Organization

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

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

A novel Robertsonian translocation in a family of Walker hounds

Guidelines for the diagnosis of fragile X syndrome

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

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

Animal model: Chromosomal fragile site expression in dogs: I. Breed specific differences

INTERFERON-INDUCIBLE FRAGILE SITE ON CHROMOSOME 16

Title Page / Table of Contents / Abstracts of Presentations at the 31 st Annual American Cytogenetic Conference

PRENATAL DIAGNOSIS OF FRAGILE X CHROMOSOME

FRAGILE X CHROMOSOME ASSOCIATED WITH FAMILIAL SEX-LINKED MENTAL RETARDATION: EXPRESSION IN FIBROBLAST CULTURE

Fragile X expression in fibroblasts

Abstracts of presentations at the Thirtieth Annual American Cytogenetics Conference

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

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