Crime and genetics conference breeds further controversy

Stage-based recipient and donor outcome in twin-to-twin transfusion syndrome treated by fetoscopic laser surgery using Solomon technique.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2024

Three-dimensional ultrasound diagnosis of adenomyosis is not associated with adverse pregnancy outcome following single thawed euploid blastocyst transfer: prospective cohort study.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2020

Prevention and treatment of pressure ulcers.

Skin therapy letter·2012

Evaluating a nurse practitioner service.

Dimensions of critical care nursing : DCCN·2011

Effects of firocoxib and tepoxalin on healing in a canine gastric mucosal injury model.

Journal of veterinary internal medicine·2009

Glutathione, cysteine, and ascorbate concentrations in clinically ill dogs and cats.

Journal of veterinary internal medicine·2009

An operational perturbation proteomics-based virtual cell model.

Nature·2026

Integrated signatures define mutational processes in prostate cancer.

Nature·2026

Advancing conflict research and response through satellite-derived data.

Nature·2026

Imaging cellular activity across all organs reveals body-wide circuits.

Nature·2026

Neocortical long-range inhibition promotes cortical synchrony and sleep.

Nature·2026

TRI-611, a selective, brain-penetrant molecular glue degrader of ALK.

Nature·2026

A Situational Assessment of the Diagnostic Landscape and Organizational Readiness to Implement Next-Generation Sequencing at Two Childhood Cancer Treatment Centers in Ghana.

Pediatric blood & cancer·2026

Case Report: Clinical and molecular genetic analysis of a patient with coexisting complete androgen insensitivity syndrome and neurofibromatosis type 1 and 15pstk + polymorphism.

Frontiers in pediatrics·2026

Three-dimensional facial gestalt analysis for three neurodevelopmental disorders: Koolen-de Vries, Jansen-de Vries and KBG syndrome.

European journal of human genetics : EJHG·2026

Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women.

Annals of medicine·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

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Crime and genetics conference breeds further controversy

Related Concept Videos

Stage-based recipient and donor outcome in twin-to-twin transfusion syndrome treated by fetoscopic laser surgery using Solomon technique.

Three-dimensional ultrasound diagnosis of adenomyosis is not associated with adverse pregnancy outcome following single thawed euploid blastocyst transfer: prospective cohort study.

Prevention and treatment of pressure ulcers.

Evaluating a nurse practitioner service.

Effects of firocoxib and tepoxalin on healing in a canine gastric mucosal injury model.

Glutathione, cysteine, and ascorbate concentrations in clinically ill dogs and cats.

An operational perturbation proteomics-based virtual cell model.

Integrated signatures define mutational processes in prostate cancer.

Advancing conflict research and response through satellite-derived data.

Imaging cellular activity across all organs reveals body-wide circuits.

Neocortical long-range inhibition promotes cortical synchrony and sleep.

TRI-611, a selective, brain-penetrant molecular glue degrader of ALK.

A Situational Assessment of the Diagnostic Landscape and Organizational Readiness to Implement Next-Generation Sequencing at Two Childhood Cancer Treatment Centers in Ghana.

Case Report: Clinical and molecular genetic analysis of a patient with coexisting complete androgen insensitivity syndrome and neurofibromatosis type 1 and 15pstk + polymorphism.

Three-dimensional facial gestalt analysis for three neurodevelopmental disorders: Koolen-de Vries, Jansen-de Vries and KBG syndrome.

Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women.

Familial short stature: genetic architecture, risk stratification, and precision management.

Shared genetic architecture between DTI-ALPS traits and neurodegenerative diseases.

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Crime and genetics conference breeds further controversy

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