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The epigenetic imprinting defect of patients with Beckwith—Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region

Journal of medical genetics, 2006-12, Vol.43 (12), p.902-907

2006

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Chromosome methylation patterns during mammalian preimplantation development

Genes & development, 1998-07, Vol.12 (14), p.2108-2113

1998

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Whole-genome methylation scan in ICF syndrome : hypomethylation of non-satellite DNA repeats D4Z4 and NBL2

Human molecular genetics, 2000-03, Vol.9 (4), p.597-604

2000

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An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome

Human molecular genetics, 1993-06, Vol.2 (6), p.731-735

1993

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The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease

American journal of human genetics, 1997, Vol.60 (1), p.72-79

1997

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DNMT3B mutations and DNA methylation defect define two types of ICF syndrome

Human mutation, 2005-01, Vol.25 (1), p.56-63

2005

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Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

Nature genetics, 1995-10, Vol.11 (2), p.144-149

1995

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Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients

Human molecular genetics, 1994-12, Vol.3 (12), p.2093-2102

1994

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XX:XY sex chromosome system with X heterochromatinization: an early stage of sex chromosome differentiation in the Neotropic electric eel Eigenmannia virescens

Cytogenetic and genome research, 2001-01, Vol.95 (1-2), p.73-78

2001

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Abnormal methylation does not prevent X inactivation in ICF patients

Cytogenetic and genome research, 1999-01, Vol.84 (3-4), p.245-252

1999

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Human Retinal Guanylate Cyclase (GUC2D) Maps to Chromosome 17p13.1

Genomics (San Diego, Calif.), 1994-07, Vol.22 (2), p.478-481

1994

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α-Satellite DNA methylation in normal individuals and in ICF patients : heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues

Human genetics, 1997-06, Vol.99 (6), p.738-745

1997

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Structure and refinement of the physical mapping of the gamma- glutamylcysteine ligase regulatory subunit (GLCLR) gene to chromosome 1p22.1 within the critically deleted region of human malignant mesothelioma

Cytogenetic and genome research, 1998-01, Vol.82 (1-2), p.91-94

1998

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No relationship between genetic instability in Bloom's syndrome and DNA hypomethylation of some major repetitive sequences

Human genetics, 1993-08, Vol.92 (1), p.57-60

1993

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Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatin

Cytogenetic and genome research, 1993, Vol.63 (1), p.11-15

1993

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Undermethylation of Alu sequences in ICF syndrome: molecular and in situ analysis

Cytogenetic and genome research, 1997-01, Vol.77 (3-4), p.308-313

1997

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The prosomal RNA-binding protein p27K is a member of the alpha-type human prosomal gene family

Molecular & general genetics, 1993-02, Vol.237 (1-2), p.193-205

1993

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Chromosomal phylogeny of Lagothrix, Brachyteles, and Cacajao

Cytogenetic and genome research, 1985-01, Vol.39 (2), p.99-104

1985

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Different reactivity of Z-DNA antibodies with human chromosomes modified by actinomycin D and 5-bromodeoxyuridine

Human genetics, 1987-02, Vol.75 (2), p.114-119

1987

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Hypomethylation of classical satellite DNA and chromosome instability in lymphoblastoid cell lines

Human genetics, 1993-07, Vol.91 (6), p.538-546

1993

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Complex evolution of sex chromosomes in Gerbillidae (Rodentia)

Cytogenetic and genome research, 1982-01, Vol.34 (1-2), p.158-167

1982

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Assignment of the human syntaxin 1B gene (STX) to chromosome 16p11.2 by fluorescence in situ hybridization

Genomics (San Diego, Calif.), 1996-09, Vol.36 (3), p.551-553

1996

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The OXA1L gene that controls cytochrome oxidase assembly maps to the 14q11.2 region of the human genome

Genomics (San Diego, Calif.), 1995-11, Vol.30 (2), p.396-398

1995

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Studies on the human chromosome 3 centromere with a newly cloned alphoid DNA probe

Human heredity, 1988, Vol.38 (3), p.156-167

1988

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The gene for the ligand binding chain of the human interferon gamma receptor

Immunogenetics (New York), 1997-01, Vol.45 (6), p.413-421

1997

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The epigenetic imprinting defect of patients with Beckwith—Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region

Chromosome methylation patterns during mammalian preimplantation development

Whole-genome methylation scan in ICF syndrome : hypomethylation of non-satellite DNA repeats D4Z4 and NBL2

An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome

The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients

XX:XY sex chromosome system with X heterochromatinization: an early stage of sex chromosome differentiation in the Neotropic electric eel Eigenmannia virescens

Abnormal methylation does not prevent X inactivation in ICF patients

Human Retinal Guanylate Cyclase (GUC2D) Maps to Chromosome 17p13.1

α-Satellite DNA methylation in normal individuals and in ICF patients : heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues

Structure and refinement of the physical mapping of the gamma- glutamylcysteine ligase regulatory subunit (GLCLR) gene to chromosome 1p22.1 within the critically deleted region of human malignant mesothelioma

No relationship between genetic instability in Bloom's syndrome and DNA hypomethylation of some major repetitive sequences

Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatin

Undermethylation of Alu sequences in ICF syndrome: molecular and in situ analysis

The prosomal RNA-binding protein p27K is a member of the alpha-type human prosomal gene family

Chromosomal phylogeny of Lagothrix, Brachyteles, and Cacajao

Different reactivity of Z-DNA antibodies with human chromosomes modified by actinomycin D and 5-bromodeoxyuridine

Hypomethylation of classical satellite DNA and chromosome instability in lymphoblastoid cell lines

Complex evolution of sex chromosomes in Gerbillidae (Rodentia)

Assignment of the human syntaxin 1B gene (STX) to chromosome 16p11.2 by fluorescence in situ hybridization

The OXA1L gene that controls cytochrome oxidase assembly maps to the 14q11.2 region of the human genome

Studies on the human chromosome 3 centromere with a newly cloned alphoid DNA probe

The gene for the ligand binding chain of the human interferon gamma receptor

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