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Developmental Biology of Uterine Glands

Biology of reproduction, 2001-11, Vol.65 (5), p.1311-1323

2001

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Endometrial development and adenogenesis in the neonatal pig: effects of estradiol valerate and the antiestrogen ICI 182,780

Biology of reproduction, 1999-07, Vol.61 (1), p.253-263

1999

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Characterization of the full fragile X syndrome mutation in fetal gametes

Nature genetics, 1997-02, Vol.15 (2), p.165-169

1997

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Cognitive effects of diarrhea, malnutrition, and Entamoeba histolytica infection on school age children in Dhaka, Bangladesh

The American journal of tropical medicine and hygiene, 2006-03, Vol.74 (3), p.475

2006

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Estrogen-induced disruption of neonatal porcine uterine development alters adult uterine function

Biology of reproduction, 2003-04, Vol.68 (4), p.1387-1893

2003

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Ovary-independent estrogen receptor expression in neonatal porcine endometrium

Biology of reproduction, 1998-04, Vol.58 (4), p.1009-1019

1998

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A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases

American journal of human genetics, 1994-08, Vol.55 (2), p.225-237

1994

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Evidence of founder chromosomes in fragile X syndrome

Nature genetics, 1992-07, Vol.1 (4), p.257-260

1992

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Expression and Molecular Characterization of Estrogen Receptor Alpha Messenger RNA in Male Reproductive Organs of Adult Goats

Biology of reproduction, 2001-05, Vol.64 (5), p.1432-1438

2001

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Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome

American journal of human genetics, 1993-10, Vol.53 (4), p.800-809

1993

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Keratinocyte growth factor expression by the bovine corpus luteum

Biology of reproduction, 1998-07, Vol.59 (1), p.77-83

1998

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Regulation of Caulobacter crescentus ilvBN gene expression

Journal of Bacteriology, 1994-06, Vol.176 (12), p.3765-3774

1994

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Neonatal estradiol exposure alters uterine morphology and endometrial transcriptional activity in prepubertal gilts

Domestic animal endocrinology, 2001-08, Vol.21 (2), p.111-125

2001

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An Extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype

Human molecular genetics, 1993-11, Vol.2 (11), p.1973-1974

1993

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Molecular genetic advances in fragile X syndrome

The Journal of pediatrics, 1993-02, Vol.122 (2), p.169-185

1993

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Expression and Molecular Characterization of Estrogen Receptor Alpha Messenger RNA in Male Reproductive Organs of Adult Goats1

Biology of reproduction, 2001-05, Vol.64 (5), p.1432-1438

2001

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Molecular heterogeneity of the fragile X syndrome

Nucleic acids research, 1991-08, Vol.19 (16), p.4355-4359

1991

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Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy

American journal of human genetics, 1992-10, Vol.51 (4), p.721-729

1992

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Isolation and characterization of ilvA, ilvBN, and ilvD mutants of Caulobacter crescentus

Journal of Bacteriology, 1991-02, Vol.173 (3), p.1259-1267

1991

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DATA CAPTURE IN THE 1990s

Photogrammetric record, 1991-04, Vol.13 (77), p.717-720

Tarleton, J.

1991

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Development of Genomic Reference Materials for Cystic Fibrosis Genetic Testing

The Journal of molecular diagnostics : JMD, 2009-05, Vol.11 (3), p.186-193

2009

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Estrogen-Induced Disruption of Neonatal Porcine Uterine Development Alters Adult Uterine Function1

Biology of reproduction, 2003-04, Vol.68 (4), p.1387-1393

2003

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The use of a new multiplex PCR assay significantly improves the rapid detection of deletions in the dystrophin gene

American journal of human genetics, 1991-08, Vol.49 (2), p.461-462

1991

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Direct analysis of the FMR-1 gene provides an explanation for an exceptional case of a fragile X negative, mentally retarded male in a fragile X family

Journal of medical genetics, 1992-12, Vol.29 (12), p.919-920

1992

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The elusive Angelman syndrome critical region

Journal of medical genetics, 1997-09, Vol.34 (9), p.714-718

1997

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Developmental Biology of Uterine Glands

Endometrial development and adenogenesis in the neonatal pig: effects of estradiol valerate and the antiestrogen ICI 182,780

Characterization of the full fragile X syndrome mutation in fetal gametes

Cognitive effects of diarrhea, malnutrition, and Entamoeba histolytica infection on school age children in Dhaka, Bangladesh

Estrogen-induced disruption of neonatal porcine uterine development alters adult uterine function

Ovary-independent estrogen receptor expression in neonatal porcine endometrium

A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases

Evidence of founder chromosomes in fragile X syndrome

Expression and Molecular Characterization of Estrogen Receptor Alpha Messenger RNA in Male Reproductive Organs of Adult Goats

Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome

Keratinocyte growth factor expression by the bovine corpus luteum

Regulation of Caulobacter crescentus ilvBN gene expression

Neonatal estradiol exposure alters uterine morphology and endometrial transcriptional activity in prepubertal gilts

An Extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype

Molecular genetic advances in fragile X syndrome

Expression and Molecular Characterization of Estrogen Receptor Alpha Messenger RNA in Male Reproductive Organs of Adult Goats1

Molecular heterogeneity of the fragile X syndrome

Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy

Isolation and characterization of ilvA, ilvBN, and ilvD mutants of Caulobacter crescentus

DATA CAPTURE IN THE 1990s

Development of Genomic Reference Materials for Cystic Fibrosis Genetic Testing

Estrogen-Induced Disruption of Neonatal Porcine Uterine Development Alters Adult Uterine Function1

The use of a new multiplex PCR assay significantly improves the rapid detection of deletions in the dystrophin gene

Direct analysis of the FMR-1 gene provides an explanation for an exceptional case of a fragile X negative, mentally retarded male in a fragile X family

The elusive Angelman syndrome critical region

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