[Development and present status of descriptive morphology of human chromosomes]

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

Replication stress links Geminin depletion to centrosome amplification.

bioRxiv : the preprint server for biology·2026

Comparative Kd analysis of the interaction between aggregation-prone Nup153 3-2 and KapN.

Journal of magnetic resonance (San Diego, Calif. : 1997)·2026

Organelle partitioning in the multi-budding yeast Aureobasidium pullulans.

Molecular biology of the cell·2026

Pronuclear Transfer and Maternal Spindle Transfer in the Mouse.

Methods in molecular biology (Clifton, N.J.)·2026

Molecular architecture and spatial organization of proteasomes in the human sperm nucleus.

Nature structural & molecular biology·2026

Resolving missing human polymorphic inversions and other complex variants from ultra-long read data.

Genome research·2026

Related Experiment Videos

[Development and present status of descriptive morphology of human chromosomes]

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].

Replication stress links Geminin depletion to centrosome amplification.

Comparative Kd analysis of the interaction between aggregation-prone Nup153 3-2 and KapN.

Organelle partitioning in the multi-budding yeast Aureobasidium pullulans.

Pronuclear Transfer and Maternal Spindle Transfer in the Mouse.

Molecular architecture and spatial organization of proteasomes in the human sperm nucleus.

Resolving missing human polymorphic inversions and other complex variants from ultra-long read data.

Related Experiment Videos

[Development and present status of descriptive morphology of human chromosomes]

Related Concept Videos

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