[Study stay at the genetic research laboratories in U.S.A]

UV absorption of Criegee intermediates: quantitative cross sections from high-level ab initio theory.

Physical chemistry chemical physics : PCCP·2018

Allelic heterogeneity of alkaptonuria in Central Europe.

European journal of human genetics : EJHG·1999

[Congenital developmental defects of the cardiovascular system from the aspect of genetic factors and dysmorphogenesis].

Bratislavske lekarske listy·1999

Molecular defects in alkaptonuria.

Cytogenetics and cell genetics·1997

The human gene for alkaptonuria (AKU) maps to chromosome 3q.

Genomics·1994

[Disorders of the cardiovascular system in congenital lentiginosis].

Ceskoslovenska pediatrie·1991

[Growth, development and prediction of body height in children with central precocious puberty after 3 years of therapy with Decapeptyl-Depot, a slow-releasing GnRH agonist].

Ceskoslovenska pediatrie·1994

[Dangers in external treatment of skin diseases in childhood].

Ceskoslovenska pediatrie·1994

[The effect of growth hormone therapy on thyroid parameters].

Ceskoslovenska pediatrie·1994

[Long-term therapy of central precocious puberty in girls with the gonadoliberin analog D-Trp-6-LHRH after prior therapy with cyproterone acetate].

Ceskoslovenska pediatrie·1994

[Improvement in the prognosis for growth in a boy with central precocious puberty and growth hormone deficiency treated concurrently with growth hormone and D-Trp-6-LHRH gonadoliberin analog].

Ceskoslovenska pediatrie·1994

[D-Trp-6 gonadotropin analog releasing hormone (Decapeptyl-Depot)-- the drug of choice in central idiopathic precocious puberty].

Ceskoslovenska pediatrie·1994

visPedigree: a comprehensive R package for tidying, analyzing, and visualizing breeding pedigrees.

Bioinformatics advances·2026

CycleMix: Gaussian mixture modeling of the cell cycle.

Bioinformatics advances·2026

TandemTwister: scalable genotyping and advanced visualization of tandem repeats.

NAR genomics and bioinformatics·2026

Clinical and Cytogenomic Characterization of Three Patients With Distal 1q43q44 Deletion: Twin Sisters With a de novo Deletion and a Patient With der(1)t(1;21)(q43;q22.3)mat.

Journal of clinical laboratory analysis·2026

HIPK4 is a novel gene associated with teratozoospermia and male infertility.

Human reproduction open·2026

Edge Preserved U-Net for chromosome edge detection.

Computational biology and chemistry·2026

Related Experiment Videos

[Study stay at the genetic research laboratories in U.S.A]

Related Concept Videos

UV absorption of Criegee intermediates: quantitative cross sections from high-level ab initio theory.

Allelic heterogeneity of alkaptonuria in Central Europe.

[Congenital developmental defects of the cardiovascular system from the aspect of genetic factors and dysmorphogenesis].

Molecular defects in alkaptonuria.

The human gene for alkaptonuria (AKU) maps to chromosome 3q.

[Disorders of the cardiovascular system in congenital lentiginosis].

[Growth, development and prediction of body height in children with central precocious puberty after 3 years of therapy with Decapeptyl-Depot, a slow-releasing GnRH agonist].

[Dangers in external treatment of skin diseases in childhood].

[The effect of growth hormone therapy on thyroid parameters].

[Long-term therapy of central precocious puberty in girls with the gonadoliberin analog D-Trp-6-LHRH after prior therapy with cyproterone acetate].

[Improvement in the prognosis for growth in a boy with central precocious puberty and growth hormone deficiency treated concurrently with growth hormone and D-Trp-6-LHRH gonadoliberin analog].

[D-Trp-6 gonadotropin analog releasing hormone (Decapeptyl-Depot)-- the drug of choice in central idiopathic precocious puberty].

visPedigree: a comprehensive R package for tidying, analyzing, and visualizing breeding pedigrees.

CycleMix: Gaussian mixture modeling of the cell cycle.

TandemTwister: scalable genotyping and advanced visualization of tandem repeats.

Clinical and Cytogenomic Characterization of Three Patients With Distal 1q43q44 Deletion: Twin Sisters With a de novo Deletion and a Patient With der(1)t(1;21)(q43;q22.3)mat.

HIPK4 is a novel gene associated with teratozoospermia and male infertility.

Edge Preserved U-Net for chromosome edge detection.

Related Experiment Videos

[Study stay at the genetic research laboratories in U.S.A]

Related Concept Videos

Related Articles