Incidence of abdominal wall defects

Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping.

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Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene.

Clinical genetics·2002

Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.

American journal of medical genetics·2001

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21.

Human molecular genetics·1996

DNA testing and genetic counseling: truth or consequences.

Wisconsin medical journal·1994

Wisconsin consanguinity studies. II: Familial adenocarcinomatosis.

American journal of medical genetics·1989

Comparison of Medium-Coverage Whole-Genome Sequencing and Chromosomal Microarray in Prenatal Testing of Absence of Heterozygosity.

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The Diagnosis and Prenatal Management of Non-RHD Alloimmunizations.

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Diagnostic Testing After Positive Cell-Free DNA Screening for Sex Chromosome Aneuploidies: Clinical and Socioeconomic Determinants.

Prenatal diagnosis·2026

Mirror Syndrome (Ballantyne Syndrome): Prenatal Diagnosis, Pathophysiology, and the Role of Fetal Therapy-A Narrative Review.

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Quantitative MRI Assessment of Gyrification and Brain Volume in Congenital Cytomegalovirus Fetuses and Postnatal Outcome.

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Parental Decision-Making and Pregnancy Outcomes After Increased First-Trimester Nuchal Translucency: A 12-Year Cohort.

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Bending-Stable Pressure Sensor Based on Natural Wood Nanofibers for Ultra-Low Detection Limit.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

The effects of different intensities of aerobic exercise for 8 weeks on neurogenesis, depression, and anxiety in young mice.

Journal of Korean biological nursing science·2026

Effects of Asymmetric Scarring in a Lumped-Mass Vocal System.

Journal of voice : official journal of the Voice Foundation·2026

Assessment and validation of the established free-running framework for cardiac function by magnetic resonance imaging at 1.5T (FAST-CMR): an international multi-center, multi-vendor study.

Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance·2026

Modulating intermolecular interactions and vibrational energy transfer in energetic systems with external electric fields.

The Journal of chemical physics·2026

Medial gastrocnemius activation during graded axial hypergravity induced by short-arm human centrifugation.

European journal of applied physiology·2026

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Incidence of abdominal wall defects

Related Concept Videos

Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping.

Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene.

Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21.

DNA testing and genetic counseling: truth or consequences.

Wisconsin consanguinity studies. II: Familial adenocarcinomatosis.

Comparison of Medium-Coverage Whole-Genome Sequencing and Chromosomal Microarray in Prenatal Testing of Absence of Heterozygosity.

The Diagnosis and Prenatal Management of Non-RHD Alloimmunizations.

Diagnostic Testing After Positive Cell-Free DNA Screening for Sex Chromosome Aneuploidies: Clinical and Socioeconomic Determinants.

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Quantitative MRI Assessment of Gyrification and Brain Volume in Congenital Cytomegalovirus Fetuses and Postnatal Outcome.

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The effects of different intensities of aerobic exercise for 8 weeks on neurogenesis, depression, and anxiety in young mice.

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Incidence of abdominal wall defects

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