Related Experiment Videos
Autosomal dominant iridogoniodysgenesis. A genetic and clinical study
Birth Defects Original Article Series
|January 1, 1982
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Adaptation and content validation of measure yourself medical outcomes profile (MYMOP) for 7-11 year-old children.
Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation·2024
Correlation of serum protein biomarkers with disease activity in psoriatic arthritis.
Expert review of clinical immunology·2020
A systematic review of randomised controlled trials evaluating the use of patient-reported outcome measures (PROMs).
Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation·2018
Designing follow-up intervals.
Statistics in medicine·2004
Dehydroascorbic acid, a blood-brain barrier transportable form of vitamin C, mediates potent cerebroprotection in experimental stroke.
Proceedings of the National Academy of Sciences of the United States of America·2001
Limb anomalies from evolutionary, developmental, and genetic perspectives.
Birth defects original article series·1996
Multisite neural tube closure in humans.
Birth defects original article series·1996
The dynamics of ciliogenesis in prepubertal mouse meiosis reveals new clues about testis maturation.
Frontiers in cell and developmental biology·2026
Somatic Cells in the Anuran Testis.
Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation·2026
Mixed evidence that dosage sensitive genes drive global dosage compensation in flour beetles.
Genome biology and evolution·2026
[Genetic analysis of a fetus with Short-rib thoracic dysplasia 8 with or without polydactyly due to variants of DYNC2I1 gene].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026
NR5A1 gene variants: variable phenotypes, new variants, and genotype-phenotype correlations.
Frontiers in endocrinology·2026
[Genetic Dystonias].
Medicina·2026