Present status of intrauterine diagnosis of genetic defects

Home visits in the Danish High Risk and Resilience Study - VIA 7: assessment of the home environment of 508 7-year-old children born to parents diagnosed with schizophrenia or bipolar disorder.

Acta psychiatrica Scandinavica·2019

Association of the missense variant p.Arg203Trp in PACS1 as a cause of intellectual disability and seizures.

Clinical genetics·2017

Inhibition of protein kinase C (PKC) response of voltage-gated calcium (Cav)2.2 channels expressed in Xenopus oocytes by Cavβ subunits.

Neuroscience·2014

The response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening study.

Journal of inherited metabolic disease·2007

Urea cycle disorders.

Clinics in liver disease·2001

Mosaic trisomy 7 in a patient with pigmentary abnormalities.

American journal of medical genetics·1999

Standalone Salpingectomy for Primary Ovarian Cancer Prevention: A Cost-Effectiveness Analysis.

American journal of obstetrics and gynecology·2026

Uptake and outcomes associated with outpatient hysterectomy in Ontario, Canada.

American journal of obstetrics and gynecology·2026

Laparoscopic modified Davydov's technique for vaginoplasty: operative steps and technical pearls.

American journal of obstetrics and gynecology·2026

Antihypertensive Treatment Escalation and Maternal Outcomes During Expectant Management of Early-Onset Preeclampsia With Severe Features.

American journal of obstetrics and gynecology·2026

Pan-genomic analysis of alternative polyadenylation reveals a 3'UTR remodeling regulatory layer controlling salt tolerance in rice.

Journal of integrative plant biology·2026

PRMT1-SFPQ regulates intron retention to control matrix gene expression during craniofacial development.

eLife·2026

Atypical Age-Related Patterns of Neural Signal Complexity in Autism Spectrum Disorder.

CNS neuroscience & therapeutics·2026

Who Are We Missing: Examining Health Insurance Coverage for Expanded Carrier Screening.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Goltz Syndrome With Large Esophageal Squamous Papillomas-A Unique Cause of Dysphagia Amenable to Endoscopic Treatment.

ACG case reports journal·2026

Characteristics of gut microbiota dysbiosis in patients with depression: a visual analysis of knowledge maps.

Frontiers in microbiology·2026

Related Experiment Videos

Present status of intrauterine diagnosis of genetic defects

Related Concept Videos

Home visits in the Danish High Risk and Resilience Study - VIA 7: assessment of the home environment of 508 7-year-old children born to parents diagnosed with schizophrenia or bipolar disorder.

Association of the missense variant p.Arg203Trp in PACS1 as a cause of intellectual disability and seizures.

Inhibition of protein kinase C (PKC) response of voltage-gated calcium (Cav)2.2 channels expressed in Xenopus oocytes by Cavβ subunits.

The response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening study.

Urea cycle disorders.

Mosaic trisomy 7 in a patient with pigmentary abnormalities.

Standalone Salpingectomy for Primary Ovarian Cancer Prevention: A Cost-Effectiveness Analysis.

Uptake and outcomes associated with outpatient hysterectomy in Ontario, Canada.

Laparoscopic modified Davydov's technique for vaginoplasty: operative steps and technical pearls.

Antihypertensive Treatment Escalation and Maternal Outcomes During Expectant Management of Early-Onset Preeclampsia With Severe Features.

Pan-genomic analysis of alternative polyadenylation reveals a 3'UTR remodeling regulatory layer controlling salt tolerance in rice.

PRMT1-SFPQ regulates intron retention to control matrix gene expression during craniofacial development.

Atypical Age-Related Patterns of Neural Signal Complexity in Autism Spectrum Disorder.

Who Are We Missing: Examining Health Insurance Coverage for Expanded Carrier Screening.

Goltz Syndrome With Large Esophageal Squamous Papillomas-A Unique Cause of Dysphagia Amenable to Endoscopic Treatment.

Characteristics of gut microbiota dysbiosis in patients with depression: a visual analysis of knowledge maps.

Related Experiment Videos

Present status of intrauterine diagnosis of genetic defects

Related Concept Videos

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