The phenotype in de novo and familial pericentric inversion 6. A problem in karyotype-phenotype correlation

[The effect of valproic acid monotherapy on behavior and cognitive performance of children with idiopathic generalized epilepsy].

Zeitschrift fur Kinder- und Jugendpsychiatrie·1995

Quantification of mitral regurgitation--comparison of the proximal flow convergence method and the jet area method.

Clinical cardiology·1995

[Residual postoperative pneumothorax: harmless radiological finding or complication-prone diagnosis?].

Schweizerische medizinische Wochenschrift·1995

Glomerular permselectivity in proteinuric patients after kidney transplantation.

The Journal of clinical investigation·1995

Killing and mutation of Chinese hamster V79 cells exposed to accelerated oxygen and neon ions.

Radiation research·1995

Growth status-dependent changes of bFGF compartmentalization and heparan sulfate structure in arterial smooth muscle cells.

European journal of cell biology·1995

Optical genome mapping improves structural variant detection and characterization in syndromic and neurogenetic disorders.

Human genetics·2026

Development of RS1-specific ACMG/AMP variant classification criteria with pilot variant curation.

Human genetics·2026

Integrating genetic, historical, and demographic evidence to reconstruct Argentina's matrilineal ancestry.

Human genetics·2026

Expected costs and benefits of genetic counselling and germline genetic testing in metastatic prostate cancer.

Human genetics·2026

From targeted SCN1A analysis to whole exome sequencing: clinical utility and novel genetic findings in a Hungarian paediatric epilepsy cohort.

Human genetics·2026

Genomic characterization of historical Jinlingnan individuals: insights into genetic continuity and trans-Eurasian signals in eastern China.

Human genetics·2026

Liver disease reveals KIF12 as a regulator of mitochondria, lysosome and cilia localisation in human cholangiocytes.

EBioMedicine·2026

Transgenerational chromosome repair in the asexual bdelloid rotifer Adineta vaga.

Science advances·2026

Site-Specific Measurement of Meiotic Crossing-Over Rate with Droplet Digital PCR.

Cold Spring Harbor protocols·2026

The periphery of nuclear speckles defines a spatially and temporally regulated compartment of long-lived intron-retained RNAs that resolves during mitosis.

Nature cell biology·2026

Whole-genome sequencing identifies a c.1282C > T missense variant in Taurine Transporter (TauT) associated with taurine-mediated dilated cardiomyopathy in a family of domestic shorthair cats.

Journal of molecular and cellular cardiology·2026

Mitochondrial genome characteristics and phylogenetic analysis of Ramaria longispora.

Mitochondrial DNA. Part B, Resources·2026

Related Experiment Videos

The phenotype in de novo and familial pericentric inversion 6. A problem in karyotype-phenotype correlation

Related Concept Videos

[The effect of valproic acid monotherapy on behavior and cognitive performance of children with idiopathic generalized epilepsy].

Quantification of mitral regurgitation--comparison of the proximal flow convergence method and the jet area method.

[Residual postoperative pneumothorax: harmless radiological finding or complication-prone diagnosis?].

Glomerular permselectivity in proteinuric patients after kidney transplantation.

Killing and mutation of Chinese hamster V79 cells exposed to accelerated oxygen and neon ions.

Growth status-dependent changes of bFGF compartmentalization and heparan sulfate structure in arterial smooth muscle cells.

Optical genome mapping improves structural variant detection and characterization in syndromic and neurogenetic disorders.

Development of RS1-specific ACMG/AMP variant classification criteria with pilot variant curation.

Integrating genetic, historical, and demographic evidence to reconstruct Argentina's matrilineal ancestry.

Expected costs and benefits of genetic counselling and germline genetic testing in metastatic prostate cancer.

From targeted SCN1A analysis to whole exome sequencing: clinical utility and novel genetic findings in a Hungarian paediatric epilepsy cohort.

Genomic characterization of historical Jinlingnan individuals: insights into genetic continuity and trans-Eurasian signals in eastern China.

Liver disease reveals KIF12 as a regulator of mitochondria, lysosome and cilia localisation in human cholangiocytes.

Transgenerational chromosome repair in the asexual bdelloid rotifer Adineta vaga.

Site-Specific Measurement of Meiotic Crossing-Over Rate with Droplet Digital PCR.

The periphery of nuclear speckles defines a spatially and temporally regulated compartment of long-lived intron-retained RNAs that resolves during mitosis.

Whole-genome sequencing identifies a c.1282C > T missense variant in Taurine Transporter (TauT) associated with taurine-mediated dilated cardiomyopathy in a family of domestic shorthair cats.

Mitochondrial genome characteristics and phylogenetic analysis of Ramaria longispora.

Related Experiment Videos

The phenotype in de novo and familial pericentric inversion 6. A problem in karyotype-phenotype correlation

Related Concept Videos

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