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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 17, 1998
Biological and clinical significance of concurrent p53 gene alterations, MDR1 gene expression, and S-phase fraction analyses in breast cancer patients treated with primary chemotherapy or radiotherapyS Chevillard, J Lebeau, P Pouillart, et al.
Nature Genetics|June 1, 1995
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severityF Piccolo, S L Roberds, M Jeanpierre, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization eventI Henry, A Puech, A Riesewijk, et al.
Seizure|May 25, 2002
So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutationV des Portes, L Abaoub, A Joannard, et al.
Human Biology|June 1, 1994
Anthropological approach to the heterogeneity of beta-thalassemia mutations in northern AfricaC Bennani, R Bouhass, P Perrin-Pecontal, et al.
Human Molecular Genetics|August 1, 1995
Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung diseaseT Attié, A Pelet, P Edery, et al.
Human Mutation|August 29, 2001
Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategyT Bienvenu, I Souville, K Poirier, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1995
The RET protooncogene in sporadic pheochromocytomas: frequent MEN 2-like mutations and new molecular defectsC Beldjord, F Desclaux-Arramond, M Raffin-Sanson, et al.
Annales De Genetique|May 20, 2000
Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardationP Billuart, J Chelly, A Carrié, et al.
Clinical Genetics|May 15, 2015
X-chromosome inactivation in female patients with Fabry diseaseL Echevarria, K Benistan, A Toussaint, et al.
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