[Genetic problems in the study of systemic congenital orthopedic diseases]

[Improving renal cancer care].

Urologiia (Moscow, Russia : 1999)·2018

A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasia.

Endocrine journal·1999

[Molecular-genetic characteristics of the deleted region of chromosome 8q24.1 in Langer-Giedion and tricho-rhino-phalangeal type I syndromes].

Genetika·1996

[Treatment of closed fractures in children].

Khirurgiia·1995

[Congenital and acquired deformities of knee joint menisci in children].

Khirurgiia·1994

A single base mutation in the type II procollagen gene (COL2A1) that converts glycine alpha 1-247 to serine in a family with late-onset spondyloepiphyseal dysplasia.

Human mutation·1994

[Atlanto-axial instability in injuries of the ligament system in children and adolescents].

Ortopediia travmatologiia i protezirovanie·1991

[Roentgenological diagnosis of dystrophic bone cysts in children].

Ortopediia travmatologiia i protezirovanie·1991

[Computerized tomography in the diagnosis and control of the effectiveness of the treatment of injuries of the Achilles tendon].

Ortopediia travmatologiia i protezirovanie·1991

[Surgical treatment of scoliosis by the Armstrong method].

Ortopediia travmatologiia i protezirovanie·1991

[Injuries of the spine and spinal cord associated with other injuries].

Ortopediia travmatologiia i protezirovanie·1991

[Supratrochanteric osteotomy of the hip in adults with dysplastic coxarthrosis].

Ortopediia travmatologiia i protezirovanie·1991

Spatial Genetic Mapping of Normal Human Prostate Tissue Identifies Epithelial Compartments Enriched for Prostate Cancer Association.

Molecular carcinogenesis·2026

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

Brain : a journal of neurology·2026

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Therapeutic advances in rare disease·2026

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Journal of human genetics·2026

Related Experiment Videos

[Genetic problems in the study of systemic congenital orthopedic diseases]

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[Improving renal cancer care].

A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasia.

[Molecular-genetic characteristics of the deleted region of chromosome 8q24.1 in Langer-Giedion and tricho-rhino-phalangeal type I syndromes].

[Treatment of closed fractures in children].

[Congenital and acquired deformities of knee joint menisci in children].

A single base mutation in the type II procollagen gene (COL2A1) that converts glycine alpha 1-247 to serine in a family with late-onset spondyloepiphyseal dysplasia.

[Atlanto-axial instability in injuries of the ligament system in children and adolescents].

[Roentgenological diagnosis of dystrophic bone cysts in children].

[Computerized tomography in the diagnosis and control of the effectiveness of the treatment of injuries of the Achilles tendon].

[Surgical treatment of scoliosis by the Armstrong method].

[Injuries of the spine and spinal cord associated with other injuries].

[Supratrochanteric osteotomy of the hip in adults with dysplastic coxarthrosis].

Spatial Genetic Mapping of Normal Human Prostate Tissue Identifies Epithelial Compartments Enriched for Prostate Cancer Association.

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

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[Genetic problems in the study of systemic congenital orthopedic diseases]

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