Related Experiment Videos
X chromosome-inactivation patterns confirm the late timing of monoamniotic-MZ twinning
American Journal of Human Genetics
|July 27, 1999
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
A child-centred measure of tooth hypersensitivity for molar incisor hypomineralisation (MIH-TH): development and psychometric evaluation.
European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry·2026
Scrolls, screens and search bars: exploring family search behaviour and the quality of online information on molar incisor hypomineralisation.
European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry·2026
Dental disease burden and management in children and young people with X-linked hypophosphataemia: a scoping review and service evaluation.
European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry·2025
A UK-based consensus on clinical decision flowcharts for managing childhood amelogenesis imperfecta in the permanent dentition.
European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry·2025
Best clinical practise guidance for the use of antibiotics in children: an EAPD policy document.
European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry·2025
Oral health care pathways for patients with epidermolysis bullosa: A position statement from the European reference network for rare skin diseases.
Journal of the European Academy of Dermatology and Venereology : JEADV·2024
Genetic data sharing by clinical laboratories in Canada: A position statement by the Canadian College of Medical Geneticists.
American journal of human genetics·2026
Robust cis-by-trans epistasis in the human plasma proteome highlights an ABO-centered interaction network.
American journal of human genetics·2026
International experiences of genomic newborn screening: Lessons from over 10,800 newborns.
American journal of human genetics·2026
A rare recurring gain-of-function variant in BMPR2 causes neurodevelopmental phenotypes in humans and flies.
American journal of human genetics·2026
A highly prevalent lupus risk haplotype increases IRF7-dependent induction of IFN-α, enhancing antiviral defense and exacerbating autoimmunity.
American journal of human genetics·2026
CanVar-UK: A collaborative platform for germline interpretation in cancer susceptibility genes.
American journal of human genetics·2026
Complete genome sequence of Helicobacter pylori strain NY43 harboring bacteriophage KHP30.
Microbiology resource announcements·2026
The shared evolutionary capacities of plasmids and extrachromosomal DNA.
Nature reviews. Genetics·2026