Related Experiment Videos
A new inherited syndrome with cardiac, cutaneous, and endocrine involvement
Mayo Clinic Proceedings
|March 1, 1986
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Progression of familial and non-familial dilated cardiomyopathy: long term follow up.
Heart (British Cardiac Society)·2003
The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas.
American journal of human genetics·2001
Characteristics of two cases with dup(15)(q11.2-q12): one of maternal and one of paternal origin.
Genetics in medicine : official journal of the American College of Medical Genetics·2001
Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma.
American journal of medical genetics·2001
Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy.
Journal of molecular and cellular cardiology·2001
Incidence and Risk Factors for Severe Postoperative Hypotension in General Care Wards.
Mayo Clinic proceedings·2026
Primary Care Management of Ileal Pouch Disorders: Diagnosis, Treatment, and Referral.
Mayo Clinic proceedings·2026
Barriers and Facilitators to Innovation: A Qualitative Study in a Non-Profit Health Care System.
Mayo Clinic proceedings·2026
Zephyr, Vega, Milo, and Bell: "Living" Art at Mayo: The Mayo Clinic Peregrine Falcon Program.
Mayo Clinic proceedings·2026
[Genetic and functional characterization of a novel KIT splicing variant in a Chinese three-generation pedigree with piebaldism].
Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences·2026
Genome-wide association study of sarcopenia index reveals sex-stratified genetic architecture.
Biology of sex differences·2026
Genetic analysis, reproductive decision-making, and pregnancy outcomes in 51 Chinese osteogenesis imperfecta families.
Journal of assisted reproduction and genetics·2026
Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.
American journal of human genetics·2026