[Congenital goiter in twins - goiter in mother]

Extended genetic testing in fetuses with sonographic skeletal system abnormalities.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2021

Maternal complications in molecularly confirmed diandric and digynic triploid pregnancies: single institution experience and literature review.

Archives of gynecology and obstetrics·2020

Maïa® trapeziometacarpal joint arthroplasty: Survival and clinical outcomes at 5 years' follow-up.

Hand surgery & rehabilitation·2019

Prenatal diagnosis of congenital myopathies and muscular dystrophies.

Clinical genetics·2016

First-trimester spontaneous pregnancy loss - molecular analysis using multiplex ligation-dependent probe amplification.

Clinical genetics·2016

[Congenital toxoplasmosis in own studies].

Wiadomosci parazytologiczne·2006

COVID-19 and pregnancy: is a "forgotten" disease still a threat?

Ginekologia polska·2026

The amniotic fluid lactate level as a possible diagnostic tool for uterine fatigue, leading to prolonged labour.

Ginekologia polska·2026

Letrozole in ectopic pregnancy: exploring a promising frontier in non-surgical therapy - a narrative review.

Ginekologia polska·2026

Foetal macrosomia - incidence, determinants and neonatal outcomes: 10-years retrospective review, 2010-2019.

Ginekologia polska·2026

Assessment of fetal growth trajectories between the second and third trimesters using INTERGROWTH-21st estimated fetal weight Z-scores.

Ginekologia polska·2026

The efficacy of microbiome transplantation in treating vaginosis and its impact on vaginosis recurrence: a meta-analysis of randomized controlled trials.

Ginekologia polska·2026

A Situational Assessment of the Diagnostic Landscape and Organizational Readiness to Implement Next-Generation Sequencing at Two Childhood Cancer Treatment Centers in Ghana.

Pediatric blood & cancer·2026

Case Report: Clinical and molecular genetic analysis of a patient with coexisting complete androgen insensitivity syndrome and neurofibromatosis type 1 and 15pstk + polymorphism.

Frontiers in pediatrics·2026

Three-dimensional facial gestalt analysis for three neurodevelopmental disorders: Koolen-de Vries, Jansen-de Vries and KBG syndrome.

European journal of human genetics : EJHG·2026

Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women.

Annals of medicine·2026

Familial short stature: genetic architecture, risk stratification, and precision management.

Frontiers in endocrinology·2026

Shared genetic architecture between DTI-ALPS traits and neurodegenerative diseases.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026

Related Experiment Videos

[Congenital goiter in twins - goiter in mother]

Related Concept Videos

Extended genetic testing in fetuses with sonographic skeletal system abnormalities.

Maternal complications in molecularly confirmed diandric and digynic triploid pregnancies: single institution experience and literature review.

Maïa® trapeziometacarpal joint arthroplasty: Survival and clinical outcomes at 5 years' follow-up.

Prenatal diagnosis of congenital myopathies and muscular dystrophies.

First-trimester spontaneous pregnancy loss - molecular analysis using multiplex ligation-dependent probe amplification.

[Congenital toxoplasmosis in own studies].

COVID-19 and pregnancy: is a "forgotten" disease still a threat?

The amniotic fluid lactate level as a possible diagnostic tool for uterine fatigue, leading to prolonged labour.

Letrozole in ectopic pregnancy: exploring a promising frontier in non-surgical therapy - a narrative review.

Foetal macrosomia - incidence, determinants and neonatal outcomes: 10-years retrospective review, 2010-2019.

Assessment of fetal growth trajectories between the second and third trimesters using INTERGROWTH-21st estimated fetal weight Z-scores.

The efficacy of microbiome transplantation in treating vaginosis and its impact on vaginosis recurrence: a meta-analysis of randomized controlled trials.

A Situational Assessment of the Diagnostic Landscape and Organizational Readiness to Implement Next-Generation Sequencing at Two Childhood Cancer Treatment Centers in Ghana.

Case Report: Clinical and molecular genetic analysis of a patient with coexisting complete androgen insensitivity syndrome and neurofibromatosis type 1 and 15pstk + polymorphism.

Three-dimensional facial gestalt analysis for three neurodevelopmental disorders: Koolen-de Vries, Jansen-de Vries and KBG syndrome.

Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women.

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Shared genetic architecture between DTI-ALPS traits and neurodegenerative diseases.

Related Experiment Videos

[Congenital goiter in twins - goiter in mother]

Related Concept Videos

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