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Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate Alleles

American journal of human genetics, 2003-02, Vol.72 (2), p.454-464

2003

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Examination of Factors Associated with Instability of the FMR1 CGG Repeat

American journal of human genetics, 1998-09, Vol.63 (3), p.776-785

1998

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The Fragile X Mental Retardation Protein FMRP Binds Elongation Factor 1A mRNA and Negatively Regulates Its Translation in Vivo

The Journal of biological chemistry, 2003-05, Vol.278 (18), p.15669-15678

2003

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Survey of the Fragile X Syndrome CGG Repeat and the Short-Tandem-Repeat and Single-Nucleotide-Polymorphism Haplotypes in an African American Population

American journal of human genetics, 2000-02, Vol.66 (2), p.480-493

2000

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FMR1 CGG-Repeat Instability in Single Sperm and Lymphocytes of Fragile-X Premutation Males

American journal of human genetics, 1999-09, Vol.65 (3), p.680-688

1999

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Neutrophil Interaction With Influenza-Infected Epithelial Cells

Blood, 1988-07, Vol.72 (1), p.142-149

1988

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Cloning the ends of size selected Sfi I fragments

American journal of medical genetics, 1991-02, Vol.38 (2-3), p.384-390

1991

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Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study-preliminary data

American journal of medical genetics, 1999-04, Vol.83 (4), p.322-325

1999

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Neutrophil interaction with influenza-infected epithelial cells

Blood, 1988-07, Vol.72 (1), p.142-149

1988

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Fragile X screening program in New York State

American journal of medical genetics, 1991-02, Vol.38 (2-3), p.251-255

1991

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Apparent FMR1 allele instability in non-fragile X males

Genetic testing, 2000, Vol.4 (3), p.241-242

2000

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New York State screening program for fragile X syndrome: A progress report

American journal of medical genetics, 1992-04, Vol.43 (1-2), p.328-332

1992

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Chromosomal localization of several families of repetitive sequences by in situ hybridization

American journal of human genetics, 1985-01, Vol.37 (1), p.114-123

1985

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Distal duplication 14q: report of three cases and further delineation of the syndrome

Human genetics, 1984-11, Vol.68 (2), p.159-164

1984

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Tissue differences in fragile X mosaics: Mosaicism in blood cells may differ greatly from skin

American journal of medical genetics, 1996-08, Vol.64 (2), p.296-301

1996

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Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection

American journal of medical genetics, 1999-04, Vol.83 (4), p.338-341

1999

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In situ nick translation of the fragile X region

American journal of medical genetics, 1988-05, Vol.30 (1-2), p.443-450

1988

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Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies

American journal of medical genetics, 1999-04, Vol.83 (4), p.342-346

1999

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Symposium on Automatic Demonstration: Held at Versailles/France, December 1968

2006

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Low frequencies of apparently fragile X chromosomes in normal control cultures: a possible explanation

Experimental cell biology, 1986, Vol.54 (1), p.40

1986

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Molecular carrier testing for the fragile X syndrome: Issues for genetic counselors

Journal of genetic counseling, 1994-09, Vol.3 (3), p.233-244

1994

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Mosaicism for the FMR1 gene influences adaptive skills development in fragile X-affected males

American journal of medical genetics, 1996-08, Vol.64 (2), p.365-369

1996

Volltextzugriff (PDF)

Cloning the ends of size selected SfiI fragments

American journal of medical genetics, 1991-01, Vol.38 (2-3), p.384-390

1991

Volltextzugriff (PDF)

Chromosal localization of several families of repetitive sequences by in situ hybridization

American journal of human genetics, 1985, Vol.37 (1), p.114-123

1985

Volltextzugriff (PDF)

Localization of Chromosome 21 Probes by in Situ Hybridization

Annals of the New York Academy of Sciences, 1985-06, Vol.450 (1), p.69-83

1985

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Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate Alleles

Examination of Factors Associated with Instability of the FMR1 CGG Repeat

The Fragile X Mental Retardation Protein FMRP Binds Elongation Factor 1A mRNA and Negatively Regulates Its Translation in Vivo

Survey of the Fragile X Syndrome CGG Repeat and the Short-Tandem-Repeat and Single-Nucleotide-Polymorphism Haplotypes in an African American Population

FMR1 CGG-Repeat Instability in Single Sperm and Lymphocytes of Fragile-X Premutation Males

Neutrophil Interaction With Influenza-Infected Epithelial Cells

Cloning the ends of size selected Sfi I fragments

Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study-preliminary data

Neutrophil interaction with influenza-infected epithelial cells

Fragile X screening program in New York State

Apparent FMR1 allele instability in non-fragile X males

New York State screening program for fragile X syndrome: A progress report

Chromosomal localization of several families of repetitive sequences by in situ hybridization

Distal duplication 14q: report of three cases and further delineation of the syndrome

Tissue differences in fragile X mosaics: Mosaicism in blood cells may differ greatly from skin

Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection

In situ nick translation of the fragile X region

Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies

Symposium on Automatic Demonstration: Held at Versailles/France, December 1968

Low frequencies of apparently fragile X chromosomes in normal control cultures: a possible explanation

Molecular carrier testing for the fragile X syndrome: Issues for genetic counselors

Mosaicism for the FMR1 gene influences adaptive skills development in fragile X-affected males

Cloning the ends of size selected SfiI fragments

Chromosal localization of several families of repetitive sequences by in situ hybridization

Localization of Chromosome 21 Probes by in Situ Hybridization

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