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The clinical value of somatic TP53 gene mutations in 1,794 patients with breast cancer

Clinical cancer research, 2006-02, Vol.12 (4), p.1157-1167

2006

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Heterozygous Germ Line hCHK2 Mutations in Li-Fraumeni Syndrome

Science (American Association for the Advancement of Science), 1999-12, Vol.286 (5449), p.2528-2531

1999

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Randomized, controlled trial of an intervention for toddlers with autism: the Early Start Denver Model

Pediatrics (Evanston), 2010-01, Vol.125 (1), p.e17-e23

2010

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Treatment of Early-Onset Schizophrenia Spectrum Disorders (TEOSS): Demographic and Clinical Characteristics

Journal of the American Academy of Child and Adolescent Psychiatry, 2007-08, Vol.46 (8), p.979-988

2007

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Germ-line mutations of TP53 in Li-Fraumeni families : An extended study of 39 families

Cancer research (Chicago, Ill.), 1997-08, Vol.57 (15), p.3245-3252

1997

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Structural Rearrangement of the Retinoblastoma Gene in Human Breast Carcinoma

Science (American Association for the Advancement of Science), 1988-10, Vol.242 (4876), p.263-266

1988

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Germ Line BAX Alterations Are Infrequent in Li-Fraumeni Syndrome

Cancer epidemiology, biomarkers & prevention, 2004-08, Vol.13 (8), p.1403-1406

2004

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BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives

European journal of cancer (1990), 2006-05, Vol.42 (8), p.1143-1150

2006

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Prediction of pathogenic mutations in patients with early-onset breast cancer by family history

The Lancet (British edition), 2003-03, Vol.361 (9363), p.1101-1102

2003

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Are There Low-Penetrance TP53 Alleles? Evidence from Childhood Adrenocortical Tumors

American journal of human genetics, 1999-10, Vol.65 (4), p.995-1006

1999

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Expression of p53 protein in infiltrating and in-situ breast carcinomas

The Journal of pathology, 1991-11, Vol.165 (3), p.203-211

1991

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Anecdotal Observation

Encyclopedia of Autism Spectrum Disorders, 2021, p.201-202

2021

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Perceptual Development

Encyclopedia of Autism Spectrum Disorders, 2021, p.3414-3423

2021

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Satellite DNA is transcribed on lampbrush chromosomes

Nature (London), 1980-02, Vol.283 (5748), p.686-688

1980

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Allelic imbalance on chromosome I in human breast cancer. II. Microsatellite repeat analysis

Genes chromosomes & cancer, 1995-01, Vol.12 (1), p.24-31

1995

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Anecdotal Observation

Encyclopedia of Autism Spectrum Disorders, 2013, p.156-157

2013

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Perceptual Development

Encyclopedia of Autism Spectrum Disorders, 2013, p.2180-2190

2013

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Preparation, labelling and detection of DNA from archival tissue sections suitable for comparative genomic hybridization

Chromosome research, 1996-02, Vol.4 (2), p.163-164

1996

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The localization of laminin mRNA and protein in the postimplantation embryo and placenta of the mouse: an in situ hybridization and immunocytochemical study

Development (Cambridge), 1988-11, Vol.104 (3), p.431-446

1988

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Identification of a rare polymorphism in the human TP53 promoter

Cancer genetics and cytogenetics, 2002-06, Vol.135 (2), p.165-172

2002

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Identification and Cloning in Yeast Artificial Chromosomes of a Region of Elevated Loss of Heterozygosity on Chromosome 1p31.1 in Human Breast Cancer

Genomics (San Diego, Calif.), 1995-11, Vol.30 (2), p.233-243

1995

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Allelic imbalance on chromosome I in human breast cancer. I. Minisatellite and rflp analysis

Genes chromosomes & cancer, 1995-01, Vol.12 (1), p.16-23

1995

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Differential expression of the mitochondrial gene cytochrome oxidase ii in benign and malignant breast tissue

The Journal of pathology, 1992-10, Vol.168 (2), p.163-168

1992

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Transposon donor plasmids, based on ColIb-P9, for use in Pseudomonas putida and a variety of other gram negative bacteria

Molecular & general genetics, 1985-01, Vol.200 (1), p.65-67

1985

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Confirmation of the copy number of chromosome 1 in interphase nuclei from paraffin sections of breast tumours by fluorescencein situ hybridization

Chromosome research, 1995-11, Vol.3 (7), p.410-416

1995

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The clinical value of somatic TP53 gene mutations in 1,794 patients with breast cancer

Heterozygous Germ Line hCHK2 Mutations in Li-Fraumeni Syndrome

Randomized, controlled trial of an intervention for toddlers with autism: the Early Start Denver Model

Treatment of Early-Onset Schizophrenia Spectrum Disorders (TEOSS): Demographic and Clinical Characteristics

Germ-line mutations of TP53 in Li-Fraumeni families : An extended study of 39 families

Structural Rearrangement of the Retinoblastoma Gene in Human Breast Carcinoma

Germ Line BAX Alterations Are Infrequent in Li-Fraumeni Syndrome

BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives

Prediction of pathogenic mutations in patients with early-onset breast cancer by family history

Are There Low-Penetrance TP53 Alleles? Evidence from Childhood Adrenocortical Tumors

Expression of p53 protein in infiltrating and in-situ breast carcinomas

Anecdotal Observation

Perceptual Development

Satellite DNA is transcribed on lampbrush chromosomes

Allelic imbalance on chromosome I in human breast cancer. II. Microsatellite repeat analysis

Anecdotal Observation

Perceptual Development

Preparation, labelling and detection of DNA from archival tissue sections suitable for comparative genomic hybridization

The localization of laminin mRNA and protein in the postimplantation embryo and placenta of the mouse: an in situ hybridization and immunocytochemical study

Identification of a rare polymorphism in the human TP53 promoter

Identification and Cloning in Yeast Artificial Chromosomes of a Region of Elevated Loss of Heterozygosity on Chromosome 1p31.1 in Human Breast Cancer

Allelic imbalance on chromosome I in human breast cancer. I. Minisatellite and rflp analysis

Differential expression of the mitochondrial gene cytochrome oxidase ii in benign and malignant breast tissue

Transposon donor plasmids, based on ColIb-P9, for use in Pseudomonas putida and a variety of other gram negative bacteria

Confirmation of the copy number of chromosome 1 in interphase nuclei from paraffin sections of breast tumours by fluorescencein situ hybridization

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