Related Experiment Videos
A recessive form of ectrodactyly, and its implications in genetic counseling
The Journal of Heredity
|January 1, 1971
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene.
American journal of human genetics·2000
Epidemiology and genetics of endemic goiter. I. Epidemiological aspects.
Israel journal of medical sciences·1983
Endemic goitre in whites and negroes: racial or social effect?
Tropical and geographical medicine·1981
Sex and age prevalence of endemic goitre: an epidemiological study.
Journal of hygiene, epidemiology, microbiology, and immunology·1981
Historical note: the extraordinary handless and footless families of Brazil - 50 years of acheiropodia.
American journal of medical genetics·1981
Genetics of acheiropodia ("the handless and footless families of Brazil"): XI. Pathologic aspects.
American journal of medical genetics·1979
Improved Genomic Resources for the swordtail cricket, Laupala kohalensis Otte 1994.
The Journal of heredity·2026
Chromosome-Level Reference Genome of the Desert Night Lizard Xantusia vigilis.
The Journal of heredity·2026
A chromosome-level genome for the spotted flying dragon (Draco maculatus).
The Journal of heredity·2026
Familial short stature: genetic architecture, risk stratification, and precision management.
Frontiers in endocrinology·2026
Shared genetic architecture between DTI-ALPS traits and neurodegenerative diseases.
Alzheimer's & dementia : the journal of the Alzheimer's Association·2026
[Analysis of clinical phenotypes and pathogenicity of a c.4476+5G>T variant of SCN1A gene in a Chinese pedigree affected with Genetic epilepsy with febrile seizures plus].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026
APOL1 kidney disease: a critical narrative review of molecular mechanisms, clinical heterogeneity, and the emerging therapeutic landscape.
International urology and nephrology·2026
Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.
Research (Washington, D.C.)·2026