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Genome-wide methylation analysis in Silver–Russell syndrome patients

Human genetics, 2015-03, Vol.134 (3), p.317-332

2015

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Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human

Human molecular genetics, 2006-04, Vol.15 (8), p.1259-1269

2006

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The primate-specific microRNA gene cluster (C19MC) is imprinted in the placenta

Human molecular genetics, 2010-09, Vol.19 (18), p.3566-3582

2010

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Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy

Neurology, 2004-05, Vol.62 (9), p.1518

2004

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The genetic aetiology of Silver–Russell syndrome

Journal of medical genetics, 2008-04, Vol.45 (4), p.193-199

2008

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A novel form of autosomal recessive pure hereditary spastic paraplegia maps to chromosome 13q14

Neurology, 2002-12, Vol.59 (12), p.1905

2002

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Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome

American journal of human genetics, 2000-01, Vol.66 (1), p.36-46

2000

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An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands

Journal of medical genetics, 1999-06, Vol.36 (6), p.457-460

1999

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Evidence That Insulin is Imprinted in the Human Yolk Sac

Diabetes (New York, N.Y.), 2001-01, Vol.50 (1), p.199-203

2001

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Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight

Journal of molecular medicine (Berlin, Germany), 2007-04, Vol.85 (4), p.379-387

2007

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An analysis of common isodisomic regions in five mUPD 16 probands

Journal of medical genetics, 1999-03, Vol.36 (3), p.204-207

1999

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Epigenotype–phenotype correlations in Silver–Russell syndrome

Journal of medical genetics, 2010-11, Vol.47 (11), p.760-768

2010

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Imprinted genes and their role in human fetal growth

Cytogenetic and genome research, 2006-03, Vol.113 (1-4), p.262-270

2006

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Expression of the insulin-like growth factors and their receptors in term placentas: A comparison between normal and IUGR births

Molecular reproduction and development, 1998-03, Vol.49 (3), p.229-235

1998

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Biallelic expression of IGFBP1 and IGFBP3, two candidate genes for the Silver-Russell syndrome

Journal of medical genetics, 2000-01, Vol.37 (1), p.65-67

2000

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The search for the gene for Silver-Russell syndrome

Acta Paediatrica, 1999-12, Vol.88 (s433), p.42-48

1999

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Epigenetic signatures of Silver–Russell syndrome

Journal of medical genetics, 2010-03, Vol.47 (3), p.150-154

2010

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Investigation of the GRB2, GRB7, and CSH1 genes as candidates for the Silver-Russell syndrome (SRS) on chromosome 17q

Journal of medical genetics, 2002-03, Vol.39 (3), p.e13-13

2002

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Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues

European journal of human genetics : EJHG, 1998-03, Vol.6 (2), p.158-164

1998

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Genetics of silver-russell syndrome

Hormone research, 1998-01, Vol.49 (Suppl 2), p.32-36

1998

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Nucleotide-sequence analysis indicates that a DNA plasmid in a diseased isolate of Ophiostoma novo-ulmi is derived by recombination between two long repeat sequences in the mitochondrial large subunit ribosomal RNA gene

Current genetics, 1995-06, Vol.28 (1), p.54-59

1995

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Skin-homing CD8 + T lymphocytes show preferential growth in vitro and suppress CD4 + T-cell proliferation in patients with early stages of cutaneous T-cell lymphoma

Acta dermato-venereologica, 2007, Vol.87 (2), p.118-126

2007

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Lack of hemizygosity for the insulin-like growth factor I receptor gene in a quantitative study of 33 Silver Russell syndrome probands and their families

European journal of human genetics : EJHG, 1997-07, Vol.5 (4), p.235-241

1997

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A common polymorphism in exon 16 of the human insulin-like growth factor-1 receptor gene (IGF1R)

Molecular and cellular probes, 1997-10, Vol.11 (5), p.381-383

1997

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Resveratrol and Ophthalmic Diseases

Nutrients, 2016-04, Vol.8 (4), p.200-200

2016

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Genome-wide methylation analysis in Silver–Russell syndrome patients

Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human

The primate-specific microRNA gene cluster (C19MC) is imprinted in the placenta

Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy

The genetic aetiology of Silver–Russell syndrome

A novel form of autosomal recessive pure hereditary spastic paraplegia maps to chromosome 13q14

Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome

An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands

Evidence That Insulin is Imprinted in the Human Yolk Sac

Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight

An analysis of common isodisomic regions in five mUPD 16 probands

Epigenotype–phenotype correlations in Silver–Russell syndrome

Imprinted genes and their role in human fetal growth

Expression of the insulin-like growth factors and their receptors in term placentas: A comparison between normal and IUGR births

Biallelic expression of IGFBP1 and IGFBP3, two candidate genes for the Silver-Russell syndrome

The search for the gene for Silver-Russell syndrome

Epigenetic signatures of Silver–Russell syndrome

Investigation of the GRB2, GRB7, and CSH1 genes as candidates for the Silver-Russell syndrome (SRS) on chromosome 17q

Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues

Genetics of silver-russell syndrome

Nucleotide-sequence analysis indicates that a DNA plasmid in a diseased isolate of Ophiostoma novo-ulmi is derived by recombination between two long repeat sequences in the mitochondrial large subunit ribosomal RNA gene

Skin-homing CD8 + T lymphocytes show preferential growth in vitro and suppress CD4 + T-cell proliferation in patients with early stages of cutaneous T-cell lymphoma

Lack of hemizygosity for the insulin-like growth factor I receptor gene in a quantitative study of 33 Silver Russell syndrome probands and their families

A common polymorphism in exon 16 of the human insulin-like growth factor-1 receptor gene (IGF1R)

Resveratrol and Ophthalmic Diseases

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