Related Experiment Videos
Genetic counseling in families at increased risk for neural tube defects
The Alabama Journal of Medical Sciences
|July 1, 1985
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
The primary erythermalgia-susceptibility gene is located on chromosome 2q31-32.
American journal of human genetics·2001
Terminal deletion of the long arm of chromosome 4 in a mother and two sons.
Clinical genetics·1996
Translating public health research into public health practice: outcomes and characteristics of successful collaborations.
American journal of preventive medicine·1996
Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes.
Journal of medical genetics·1995
Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21.
Cytogenetics and cell genetics·1995
Congenital heart disease in infants with Down's syndrome.
Southern medical journal·1994
LRP12 CGG Repeat Expansions in Patients With Adult-Onset Non-5q Spinal Muscular Atrophy.
Neurology. Genetics·2026
[National Protocol for the Diagnosis and Management of Stickler syndrome: Summary for the attending physician].
Journal francais d'ophtalmologie·2026
Synergistic Variants in C-terminal Binding Protein 1 and Alkaline Phosphatase Lead to Mandibular Hypoplasia Through Impaired Wnt Signaling: An Oligogenic Model.
bioRxiv : the preprint server for biology·2026
Point mutations and complex variants impact gene expression and addiction-related behaviors in Heterogeneous Stock rats.
bioRxiv : the preprint server for biology·2026
Developmental Cerebellar Pathology in Mouse Models of SCN2A Premature Termination Codon Variants.
bioRxiv : the preprint server for biology·2026