Related Experiment Videos
A further study on the family with anomalous inheritance of haptoglobin types
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Usefulness of Silent MR Angiography for Intracranial Aneurysms Treated with a Flow-Diverter Device.
AJNR. American journal of neuroradiology·2019
Endobronchial Topical Amphotericin B Instillation for Pulmonary Chromomycosis After Lung Transplantation: A Case Report.
Transplantation proceedings·2018
Non-Contrast-Enhanced Silent Scan MR Angiography of Intracranial Anterior Circulation Aneurysms Treated with a Low-Profile Visualized Intraluminal Support Device.
AJNR. American journal of neuroradiology·2017
Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction.
Jinrui idengaku zasshi. The Japanese journal of human genetics·1991
Rapid detection of a point mutation in thyroid-stimulating hormone beta-subunit gene causing congenital isolated thyroid-stimulating hormone deficiency.
Jinrui idengaku zasshi. The Japanese journal of human genetics·1991
Biochemical characteristics of glucose-6-phosphate dehydrogenase variants among the Malays of Singapore with report of a new non-deficient (GdSingapore) and three deficient variants.
Jinrui idengaku zasshi. The Japanese journal of human genetics·1991
Similar proportion of sporadic cases in cytochrome b558 negative chronic granulomatous disease and Duchenne muscular dystrophy.
Jinrui idengaku zasshi. The Japanese journal of human genetics·1991
The MspI restriction fragment length polymorphism of human aldolase B gene on chromosome 9q21.3-q22.2.
Jinrui idengaku zasshi. The Japanese journal of human genetics·1991
The prevalence at birth of cogenital malformations at a maternity hospital in Osaka City, 1948-1990.
Jinrui idengaku zasshi. The Japanese journal of human genetics·1991
Delving into the clinical and genetic spectrum of NLSDM: A case study.
Journal of neuromuscular diseases·2026
Mutation Spectrum and Novel Rare Variants in a Han Chinese Hearing Loss Cohort Using a Tiered Sequencing Strategy.
Molecular genetics & genomic medicine·2026