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Cancer Research|June 11, 1998
Genomic changes in endometrial polyps associated with tamoxifen show no evidence for its action as an external carcinogenP Dal Cin, D Timmerman, I Van den Berghe, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|May 18, 2013
Breast cancer phenotype, nodal status and palpability may be useful in the detection of overdiagnosed screening-detected breast cancersO Brouckaert, A Schoneveld, C Truyers, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlationsM R Nelen, H Kremer, I B Konings, et al.
Nature Genetics|March 10, 2001
Constitutively activating mutation in WASP causes X-linked severe congenital neutropeniaK Devriendt, A S Kim, G Mathijs, et al.
Journal of Medical Genetics|September 18, 2007
Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)N M C Maas, G Van Buggenhout, F Hannes, et al.
American Journal of Human Genetics|May 1, 1996
Mental status of females with an FMR1 gene full mutationB B de Vries, A M Wiegers, A P Smits, et al.
Molecular Psychiatry|February 25, 2009
Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autismF Laumonnier, C Shoubridge, C Antar, et al.
Breast Cancer Research and Treatment|November 22, 2017
Body mass index, age at breast cancer diagnosis, and breast cancer subtype: a cross-sectional studyO Brouckaert, K Van Asten, A Laenen, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 26, 2011
Ovarian cancer arising in endometrioid cysts: ultrasound findingsA C Testa, D Timmerman, C Van Holsbeke, et al.
American Journal of Medical Genetics. Part A|December 8, 2005
Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): a possible locus for Fryns syndromeS Kantarci, D Casavant, C Prada, et al.
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