[Prenatal diagnosis of hereditary diseases]

Personality traits as an endophenotype in genetic studies on suicidality in bipolar disorder.

Acta neuropsychiatrica·2016

[Detection of anti-Borna disease virus antibodies in patients hospitalized in psychiatric hospitals located in the mid-Western region of Poland].

Psychiatria polska·2002

Polymorphisms in the dopamine, serotonin, and norepinephrine transporter genes and their relationship to temperamental dimensions measured by the Temperament and Character Inventory in healthy volunteers.

Neuropsychobiology·2001

[Genetic factors in the etiology of anorexia nervosa].

Psychiatria polska·2001

Effects of continuous and pulsed 2450-MHz radiation on spontaneous lymphoblastoid transformation of human lymphocytes in vitro.

Bioelectromagnetics·1992

An automated dosimetry system for microwave and thermal exposure of biological samples in vitro.

Health physics·1989

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

Clinicopathologic and recurrence characteristics of leiomyoma with bizarre nuclei, which is rare type of uterine smooth macule tumors.

Ginekologia polska·2026

Clinical value of intraoperative frozen section in the surgical management of ovarian tumors: diagnostic accuracy and correlation with final histopathology.

Ginekologia polska·2026

Serum BMP8B levels in women with polycystic ovary syndrome: a case-control study.

Ginekologia polska·2026

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Pediatrics international : official journal of the Japan Pediatric Society·2026

Proteome-wide QTL mapping enables gene-protein-phenotype metabolic network construction in a genetically diverse MASLD mouse model.

bioRxiv : the preprint server for biology·2026

Sequence determinants of pathogenicity in glucose-6-phosphatase linked to glycogen storage disease type 1a.

bioRxiv : the preprint server for biology·2026

Estimating the Penetrance of PRNP Mutations in Chinese Prion Disease Patients based on the Genome Databases.

Genomics, proteomics & bioinformatics·2026

Genome-wide linkage and association mapping identified a novel candidate gene, TaGLK-A1, underlying fructan content in wheat grain.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2026

Deletion of ARPKD-associated Pkhd1 gene in mice results in decreased Tfap2b expression and eye abnormalities.

Nature communications·2026

Related Experiment Videos

[Prenatal diagnosis of hereditary diseases]

Related Concept Videos

Personality traits as an endophenotype in genetic studies on suicidality in bipolar disorder.

[Detection of anti-Borna disease virus antibodies in patients hospitalized in psychiatric hospitals located in the mid-Western region of Poland].

Polymorphisms in the dopamine, serotonin, and norepinephrine transporter genes and their relationship to temperamental dimensions measured by the Temperament and Character Inventory in healthy volunteers.

[Genetic factors in the etiology of anorexia nervosa].

Effects of continuous and pulsed 2450-MHz radiation on spontaneous lymphoblastoid transformation of human lymphocytes in vitro.

An automated dosimetry system for microwave and thermal exposure of biological samples in vitro.

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.

Clinicopathologic and recurrence characteristics of leiomyoma with bizarre nuclei, which is rare type of uterine smooth macule tumors.

Clinical value of intraoperative frozen section in the surgical management of ovarian tumors: diagnostic accuracy and correlation with final histopathology.

Serum BMP8B levels in women with polycystic ovary syndrome: a case-control study.

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Proteome-wide QTL mapping enables gene-protein-phenotype metabolic network construction in a genetically diverse MASLD mouse model.

Sequence determinants of pathogenicity in glucose-6-phosphatase linked to glycogen storage disease type 1a.

Estimating the Penetrance of PRNP Mutations in Chinese Prion Disease Patients based on the Genome Databases.

Genome-wide linkage and association mapping identified a novel candidate gene, TaGLK-A1, underlying fructan content in wheat grain.

Deletion of ARPKD-associated Pkhd1 gene in mice results in decreased Tfap2b expression and eye abnormalities.

Related Experiment Videos

[Prenatal diagnosis of hereditary diseases]

Related Concept Videos

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