A not-so-"new" mental retardation syndrome

SRPK3 Is Essential for Cognitive and Ocular Development in Humans and Zebrafish, Explaining X-Linked Intellectual Disability.

Annals of neurology·2024

Risk and Resilience Variants in the Retinoic Acid Metabolic and Developmental Pathways Associated with Risk of FASD Outcomes.

Biomolecules·2024

Molecular characterization of 13 patients with PIK3CA-related overgrowth spectrum using a targeted deep sequencing approach.

American journal of medical genetics. Part A·2023

Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disability.

Research square·2023

Dietary Intake Patterns and Lifestyle Behaviors of Pregnant Women Living in a Manitoba First Nations Community: Implications for Fetal Alcohol Spectrum Disorder.

Nutrients·2022

Utility of Measuring Fetal Cavum Septum Pellucidum (CSP) Width During Routine Obstetrical Ultrasound for Improving Diagnosis of 22q11.2 Deletion Syndrome: A Case-Control Study.

The application of clinical genetics·2022

Defects of blastogenesis.

American journal of medical genetics·2002

Malformations of the craniofacial region: evolutionary, embryonic, genetic, and clinical perspectives.

American journal of medical genetics·2002

Limb anomalies: Developmental and evolutionary aspects.

American journal of medical genetics·2002

Molecular etiology of gut malformations and diseases.

American journal of medical genetics·2002

Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome).

American journal of medical genetics·2002

Three cases of tetrasomy 9p.

American journal of medical genetics·2002

Klazomania Refractory to Electroconvulsive Therapy: A Rare Case Report.

The journal of ECT·2026

Case Report: Polycythemia vera presenting as persistent unexplained low-grade fever.

Frontiers in medicine·2026

AI's top startups are barely publishing their research.

Science (New York, N.Y.)·2026

Lost in Translation.

Journal of the American Academy of Child and Adolescent Psychiatry·2026

Prosopometamorphopsia as an Unusual Presentation of Cerebral Venous Sinus Thrombosis in a 33-Year-Old Filipino: A Case Report.

Case reports in neurology·2026

Related Experiment Videos

A not-so-"new" mental retardation syndrome

Related Concept Videos

SRPK3 Is Essential for Cognitive and Ocular Development in Humans and Zebrafish, Explaining X-Linked Intellectual Disability.

Risk and Resilience Variants in the Retinoic Acid Metabolic and Developmental Pathways Associated with Risk of FASD Outcomes.

Molecular characterization of 13 patients with PIK3CA-related overgrowth spectrum using a targeted deep sequencing approach.

Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disability.

Dietary Intake Patterns and Lifestyle Behaviors of Pregnant Women Living in a Manitoba First Nations Community: Implications for Fetal Alcohol Spectrum Disorder.

Utility of Measuring Fetal Cavum Septum Pellucidum (CSP) Width During Routine Obstetrical Ultrasound for Improving Diagnosis of 22q11.2 Deletion Syndrome: A Case-Control Study.

Defects of blastogenesis.

Malformations of the craniofacial region: evolutionary, embryonic, genetic, and clinical perspectives.

Limb anomalies: Developmental and evolutionary aspects.

Molecular etiology of gut malformations and diseases.

Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome).

Three cases of tetrasomy 9p.

Klazomania Refractory to Electroconvulsive Therapy: A Rare Case Report.

Case Report: Polycythemia vera presenting as persistent unexplained low-grade fever.

AI's top startups are barely publishing their research.

Lost in Translation.

Prosopometamorphopsia as an Unusual Presentation of Cerebral Venous Sinus Thrombosis in a 33-Year-Old Filipino: A Case Report.

Related Experiment Videos

A not-so-"new" mental retardation syndrome

Related Concept Videos

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