Recent developments in the understanding of the aetiology of neural tube defects

Apparent prevention of neural tube defects by periconceptional vitamin supplementation. 1981.

International journal of epidemiology·2011

A 46,XX fetus with external female and internal male genitalia, facial dysmorphic features and mildly dilated lateral ventricles of the brain: a new syndrome?

Clinical dysmorphology·2001

Physical and transcript map of the dominant optic atrophy (OPA1) gene critical region at 3q28-q29.

Genomics·2001

Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomalies.

Genomics·1999

Dominant optic atrophy. Refining the clinical diagnostic criteria in light of genetic linkage studies.

Ophthalmology·1999

Altered smooth muscle development and innervation in the lower genitourinary and gastrointestinal tract of the male human fetus with myelomeningocele.

The Journal of urology·1998

Monochorionic dizygotic twins with discordant genetic findings and congenital malformations.

Clinical dysmorphology·2026

Clinical spectrum of acyl-CoA synthetase family member 3-related combined malonic and methylmalonic aciduria: insights from four cases.

Clinical dysmorphology·2026

Oculoskeletodental syndrome: expansion and review of the clinical and molecular phenotype.

Clinical dysmorphology·2026

Criminal Legal System Involvement During Adolescence as a Social Determinant of Adulthood Body Mass Index?

The Journal of adolescent health : official publication of the Society for Adolescent Medicine·2026

Histochemical staining optimization of a sperm chromatin dispersion test for the evaluation of DNA fragmentation in bovine spermatozoa.

Biotechnic & histochemistry : official publication of the Biological Stain Commission·2026

Phenotyping and hierarchical clustering in genetically unresolved DSD identifies distinct multisystem clinical subgroups-a DSDgene study.

Journal of the Endocrine Society·2026

Von Hippel-Lindau syndrome presenting as a lateral ventricular space-occupying lesion: a case report.

Frontiers in oncology·2026

Reverse Cascade Genetic Screening for Revealing New Cases of Familial Hypercholesterolemia in Russia: Pilot Project.

Frontiers in bioscience (Scholar edition)·2026

Resistance phenotyping and kdr genotyping in Aedes aegypti and Aedes albopictus from Thailand.

Acta tropica·2026

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Recent developments in the understanding of the aetiology of neural tube defects

Related Concept Videos

Apparent prevention of neural tube defects by periconceptional vitamin supplementation. 1981.

A 46,XX fetus with external female and internal male genitalia, facial dysmorphic features and mildly dilated lateral ventricles of the brain: a new syndrome?

Physical and transcript map of the dominant optic atrophy (OPA1) gene critical region at 3q28-q29.

Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomalies.

Dominant optic atrophy. Refining the clinical diagnostic criteria in light of genetic linkage studies.

Altered smooth muscle development and innervation in the lower genitourinary and gastrointestinal tract of the male human fetus with myelomeningocele.

Monochorionic dizygotic twins with discordant genetic findings and congenital malformations.

Clinical spectrum of acyl-CoA synthetase family member 3-related combined malonic and methylmalonic aciduria: insights from four cases.

Oculoskeletodental syndrome: expansion and review of the clinical and molecular phenotype.

Criminal Legal System Involvement During Adolescence as a Social Determinant of Adulthood Body Mass Index?

Histochemical staining optimization of a sperm chromatin dispersion test for the evaluation of DNA fragmentation in bovine spermatozoa.

Phenotyping and hierarchical clustering in genetically unresolved DSD identifies distinct multisystem clinical subgroups-a DSDgene study.

Von Hippel-Lindau syndrome presenting as a lateral ventricular space-occupying lesion: a case report.

Reverse Cascade Genetic Screening for Revealing New Cases of Familial Hypercholesterolemia in Russia: Pilot Project.

Resistance phenotyping and kdr genotyping in Aedes aegypti and Aedes albopictus from Thailand.

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Recent developments in the understanding of the aetiology of neural tube defects

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