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The role of genetic factors in age at natural menopause

Human reproduction (Oxford), 2001-09, Vol.16 (9), p.2014-2018

2001

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A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q

American journal of human genetics, 2003-05, Vol.72 (5), p.1251-1260

2003

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Numerical chromosomal abnormalities in equine embryos produced in vivo and in vitro

Molecular reproduction and development, 2005-09, Vol.72 (1), p.77-87

2005

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Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification

Clinical genetics, 2007-08, Vol.72 (2), p.122-129

2007

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Genome-wide linkage in a large dutch consanguineous family maps a locus for intracranial aneurysms to chromosome 2p13

Stroke (1970), 2004-10, Vol.35 (10), p.2276-2281

2004

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Neuregulin 1: genetic support for schizophrenia subtypes

Molecular psychiatry, 2004-12, Vol.9 (12), p.1061-1063

2004

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Intracytoplasmic sperm injection (ICSI) and chromosomally abnormal spermatozoa

Human reproduction (Oxford), 1997-04, Vol.12 (4), p.752-754

1997

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Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications

American journal of human genetics, 1989-12, Vol.45 (6), p.835-847

1989

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Identification of a new copper metabolism gene by positional cloning in a purebred dog population

Human molecular genetics, 2002-01, Vol.11 (2), p.165-173

2002

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Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients

Genes and immunity, 2004-05, Vol.5 (3), p.215-220

2004

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The effect of breed and intrauterine crowding on fetal erythropoiesis on day 35 of gestation in swine

Journal of animal science, 2003-09, Vol.81 (9), p.2352

2003

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A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21

Clinical genetics, 2009-05, Vol.75 (5), p.490-493

2009

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A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

Nature (London), 1985-10, Vol.317 (6037), p.542-544

1985

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Genetic Mapping of the Copper Toxicosis Locus in Bedlington Terriers to Dog Chromosome 10, in a Region Syntenic to Human Chromosome Region 2p13–p16

Human molecular genetics, 1999-03, Vol.8 (3), p.501-507

1999

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Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q

Oncogene, 1991-09, Vol.6 (9), p.1705-1711

1991

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Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations

Journal of medical genetics, 1989-09, Vol.26 (9), p.553-559

1989

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The PIP5K2A and RGS4 genes are differentially associated with deficit and non‐deficit schizophrenia

Genes, brain and behavior, 2007-03, Vol.6 (2), p.113-119

2007

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Ringo, a Golden Retriever Muscular Dystrophy (GRMD) dog with absent dystrophin but normal strength

Neuromuscular disorders : NMD, 2008-11, Vol.18 (11), p.892-893

2008

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Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations

Cytogenetic and genome research, 2006-01, Vol.115 (3-4), p.254-261

2006

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Polymorphic Detection of a Parthenogenetic Maternal and Double Paternal Contribution to a 46,XX/46,XY Hermaphrodite

American journal of human genetics, 1998-04, Vol.62 (4), p.937-940

1998

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Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours

Human genetics, 1988-12, Vol.81 (1), p.41-48

1988

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The genetic analysis of cancer

Journal of internal medicine, 1998-06, Vol.243 (6), p.413-417

1998

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Uterine environment and breed effects on erythropoiesis and liver protein secretion in late embryonic and early fetal swine

Biology of reproduction, 1998-04, Vol.58 (4), p.911-918

1998

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Sperm analysis in a subfertile male with a Y;16 translocation, using four-color FISH

Cytogenetic and genome research, 1999-01, Vol.84 (1-2), p.67-72

1999

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The tissue transglutaminase gene is not a primary factor predisposing to celiac disease

The American journal of gastroenterology, 2001-12, Vol.96 (12), p.3337-3340

2001

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The role of genetic factors in age at natural menopause

A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q

Numerical chromosomal abnormalities in equine embryos produced in vivo and in vitro

Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification

Genome-wide linkage in a large dutch consanguineous family maps a locus for intracranial aneurysms to chromosome 2p13

Neuregulin 1: genetic support for schizophrenia subtypes

Intracytoplasmic sperm injection (ICSI) and chromosomally abnormal spermatozoa

Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications

Identification of a new copper metabolism gene by positional cloning in a purebred dog population

Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients

The effect of breed and intrauterine crowding on fetal erythropoiesis on day 35 of gestation in swine

A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21

A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

Genetic Mapping of the Copper Toxicosis Locus in Bedlington Terriers to Dog Chromosome 10, in a Region Syntenic to Human Chromosome Region 2p13–p16

Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q

Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations

The PIP5K2A and RGS4 genes are differentially associated with deficit and non‐deficit schizophrenia

Ringo, a Golden Retriever Muscular Dystrophy (GRMD) dog with absent dystrophin but normal strength

Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations

Polymorphic Detection of a Parthenogenetic Maternal and Double Paternal Contribution to a 46,XX/46,XY Hermaphrodite

Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours

The genetic analysis of cancer

Uterine environment and breed effects on erythropoiesis and liver protein secretion in late embryonic and early fetal swine

Sperm analysis in a subfertile male with a Y;16 translocation, using four-color FISH

The tissue transglutaminase gene is not a primary factor predisposing to celiac disease

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