Genetic landmarks through philately--Thomas Hunt Morgan (1866-1945)

The Manitoba Youth Justice Program: empowering and supporting youth with FASD in conflict with the law.

Biochemistry and cell biology = Biochimie et biologie cellulaire·2017

Correlates of age at diagnosis of autism spectrum disorders in six Canadian regions.

Chronic diseases and injuries in Canada·2012

Variable expressivity of a novel mutation in the SCN1A gene leading to an autosomal dominant seizure disorder.

Seizure·2011

A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders.

Clinical genetics·2010

Management of cleft lip and palate: a team approach.

Canadian family physician Medecin de famille canadien·2010

Genetic implications and health consequences following the Chernobyl nuclear accident.

Clinical genetics·2010

The First Case of Isolated Uterine Atony as the Only Symptom in an Individual With ACTG2-Associated Visceral Myopathy.

Clinical genetics·2026

Sotos and Malan Syndromes in Childhood: Molecular and Clinical Findings From a Nationwide Cohort of 48 Patients.

Clinical genetics·2026

Genetic Architecture of Pediatric Cardiomyopathies Assessed by Whole-Exome Sequencing: Insights Into Early-Onset and Syndromic Forms.

Clinical genetics·2026

Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.

Clinical genetics·2026

Surviving Males With PORCN Variants: Expanding the Clinical, Molecular, and Mechanistic Spectrum.

Clinical genetics·2026

A De Novo DHX16 Variant Associated With Neuromuscular Oculoauditory Syndrome Regulates Pre-mRNA Splicing In Vitro.

Clinical genetics·2026

Omphacinon (unripe olive oil) as a traditional Mediterranean medicinal carrier: an ethnopharmacological appraisal.

Frontiers in pharmacology·2026

(Re)weaving intimacies with 'Āina for our past, present, and future.

Frontiers in public health·2026

Screening strategies for Chagas Disease: evaluation of a field diagnostic algorithm in Santiago del Estero

Revista de la Facultad de Ciencias Medicas (Cordoba, Argentina)·2026

Mental models and conceptual complexity in medicine

Revista de la Facultad de Ciencias Medicas (Cordoba, Argentina)·2026

The MLLT3 YEATS domain binds histone marks (H3K9/18/27ac/cr) and ncRNA (7SK), linking transcription and RNA signaling to regulate hematopoiesis.

Cell reports·2026

Comparing Self-Reports, Pill Counts, and Electronic Devices in Assessing Antiretroviral Therapy Adherence and its Association With Viral Suppression in Adolescents Living With HIV.

Journal of acquired immune deficiency syndromes (1999)·2026

Related Experiment Videos

Genetic landmarks through philately--Thomas Hunt Morgan (1866-1945)

Related Concept Videos

The Manitoba Youth Justice Program: empowering and supporting youth with FASD in conflict with the law.

Correlates of age at diagnosis of autism spectrum disorders in six Canadian regions.

Variable expressivity of a novel mutation in the SCN1A gene leading to an autosomal dominant seizure disorder.

A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders.

Management of cleft lip and palate: a team approach.

Genetic implications and health consequences following the Chernobyl nuclear accident.

The First Case of Isolated Uterine Atony as the Only Symptom in an Individual With ACTG2-Associated Visceral Myopathy.

Sotos and Malan Syndromes in Childhood: Molecular and Clinical Findings From a Nationwide Cohort of 48 Patients.

Genetic Architecture of Pediatric Cardiomyopathies Assessed by Whole-Exome Sequencing: Insights Into Early-Onset and Syndromic Forms.

Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.

Surviving Males With PORCN Variants: Expanding the Clinical, Molecular, and Mechanistic Spectrum.

A De Novo DHX16 Variant Associated With Neuromuscular Oculoauditory Syndrome Regulates Pre-mRNA Splicing In Vitro.

Omphacinon (unripe olive oil) as a traditional Mediterranean medicinal carrier: an ethnopharmacological appraisal.

(Re)weaving intimacies with 'Āina for our past, present, and future.

Screening strategies for Chagas Disease: evaluation of a field diagnostic algorithm in Santiago del Estero

Mental models and conceptual complexity in medicine

The MLLT3 YEATS domain binds histone marks (H3K9/18/27ac/cr) and ncRNA (7SK), linking transcription and RNA signaling to regulate hematopoiesis.

Comparing Self-Reports, Pill Counts, and Electronic Devices in Assessing Antiretroviral Therapy Adherence and its Association With Viral Suppression in Adolescents Living With HIV.

Related Experiment Videos

Genetic landmarks through philately--Thomas Hunt Morgan (1866-1945)

Related Concept Videos

Related Articles