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Clinical Dysmorphology|August 5, 1998
Clinical characteristics associated with dup17(q24q25.1) in a mosaic mother and two non-mosaic daughtersD Babovic-Vuksanovic, J A Westman, S M Jalal, et al.Familial Cancer|April 6, 2012
Mutation screening of RAD51C in high-risk breast and ovarian cancer familiesWenping Lu, Xianshu Wang, Hongsheng Lin, et al.Pathology|April 29, 2017
Non-BRCA familial breast cancer: review of reported pathology and molecular findingsMichael G Keeney, Fergus J Couch, Daniel W Visscher, et al.Journal of Inherited Metabolic Disease|May 7, 2005
Selective antibody immune deficiency in a patient with Smith-Lemli-Opitz syndromeD Babovic-Vuksanovic, R M Jacobson, N M Lindor, et al.American Journal of Medical Genetics|December 31, 1997
De novo 16p deletion: ATR-16 syndromeN M Lindor, M G Valdes, M Wick, et al.American Journal of Medical Genetics|March 4, 2000
Rothmund-Thomson syndrome due to RECQ4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndromeN M Lindor, Y Furuichi, S Kitao, et al.Annals of Internal Medicine|January 15, 1995
Genetic testing in the diagnosis and management of multiple endocrine neoplasia type IIG A Ledger, S Khosla, N M Lindor, et al.Journal of Vascular Surgery|April 9, 2004
LEOPARD syndrome: a new polyaneurysm association and an update on the molecular genetics of the diseaseMarineh Yagubyan, Jean M Panneton, Noralane M Lindor, et al.Mayo Clinic Proceedings|July 1, 1997
A new autosomal dominant disorder of pyogenic sterile arthritis, pyoderma gangrenosum, and acne: PAPA syndromeN M Lindor, T M Arsenault, H Solomon, et al.Journal of Immigrant and Minority Health|June 9, 2018
Current Approaches to Cancer Genetic Counseling Services for Spanish-Speaking PatientsBianca Augusto, Monica L Kasting, Fergus J Couch, et al.Pageof 32