[Does medical progress entail deterioration of our genetic heritage?]

Glaucoma-lens ectopia-microspherophakia-stiffness-shortness (GEMSS) syndrome: a dominant disease with manifestations of Weill-Marchesani syndromes.

American journal of medical genetics·1992

Prenatal diagnosis of cystic hygroma and chorioangioma in the Wolf-Hirschhorn syndrome.

Prenatal diagnosis·1991

Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality--a new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs.

American journal of medical genetics·1990

Rieger anomaly and uveal coloboma with associated anomalies. Third observation of a rare oculo-palato-osseous syndrome--the Abruzzo-Erikson syndrome.

Ophthalmic paediatrics and genetics·1990

[Heredity in congenital dislocation of the hip].

Acta orthopaedica Belgica·1990

[An example of detection of heterozygotes and antenatal diagnosis in four families with anhidrotic ectodermal dysplasia].

Annales de pediatrie·1990

[Retinal intoxication with tamoxifen treatment for breast cancer].

Revue medicale de Liege·2026

[Volontary poisoning with yew ( Taxus baccata) : a fatal case].

Revue medicale de Liege·2026

[Pseudotumor on metal debris after total hip arthroplasty].

Revue medicale de Liege·2026

[Management of post-traumatic tibiotalar osteoarthritis following a failed osteosynthesis : retrograde plantar nailing].

Revue medicale de Liege·2026

[Femoral neck stress fracture in a young female runner].

Revue medicale de Liege·2026

[Arthroscopy of the hip : modern times surgery].

Revue medicale de Liege·2026

Yunis Varon Syndrome: Characteristic Limb Abnormalities and Refining of the Phenotype.

American journal of medical genetics. Part A·2026

Genetic control of local mutation rates.

Proceedings of the National Academy of Sciences of the United States of America·2026

Deep Sequencing of Hepatitis B Virus Reveals Clinically Relevant Low-Frequency Variants Among People Living with HIV in Botswana.

Viruses·2026

Diverse Genomic Mechanisms of cfiA Activation in Carbapenem-Resistant Bacteroides fragilis Clinical Isolates from Korea.

Antibiotics (Basel, Switzerland)·2026

Updating the RZooRoH Package for the Analysis of Inbreeding, Identity-By-Descent and Relatedness From Genomic Data.

Molecular ecology resources·2026

A single-cell transcriptome atlas reveals paradoxical monoallelic expression of RNA editing and heterozygous SNPs.

Nucleic acids research·2026

Related Experiment Videos

[Does medical progress entail deterioration of our genetic heritage?]

Related Concept Videos

Glaucoma-lens ectopia-microspherophakia-stiffness-shortness (GEMSS) syndrome: a dominant disease with manifestations of Weill-Marchesani syndromes.

Prenatal diagnosis of cystic hygroma and chorioangioma in the Wolf-Hirschhorn syndrome.

Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality--a new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs.

Rieger anomaly and uveal coloboma with associated anomalies. Third observation of a rare oculo-palato-osseous syndrome--the Abruzzo-Erikson syndrome.

[Heredity in congenital dislocation of the hip].

[An example of detection of heterozygotes and antenatal diagnosis in four families with anhidrotic ectodermal dysplasia].

[Retinal intoxication with tamoxifen treatment for breast cancer].

[Volontary poisoning with yew ( Taxus baccata) : a fatal case].

[Pseudotumor on metal debris after total hip arthroplasty].

[Management of post-traumatic tibiotalar osteoarthritis following a failed osteosynthesis : retrograde plantar nailing].

[Femoral neck stress fracture in a young female runner].

[Arthroscopy of the hip : modern times surgery].

Yunis Varon Syndrome: Characteristic Limb Abnormalities and Refining of the Phenotype.

Genetic control of local mutation rates.

Deep Sequencing of Hepatitis B Virus Reveals Clinically Relevant Low-Frequency Variants Among People Living with HIV in Botswana.

Diverse Genomic Mechanisms of cfiA Activation in Carbapenem-Resistant Bacteroides fragilis Clinical Isolates from Korea.

Updating the RZooRoH Package for the Analysis of Inbreeding, Identity-By-Descent and Relatedness From Genomic Data.

A single-cell transcriptome atlas reveals paradoxical monoallelic expression of RNA editing and heterozygous SNPs.

Related Experiment Videos

[Does medical progress entail deterioration of our genetic heritage?]

Related Concept Videos

Related Articles