[Prenatal diagnosis of hereditary diseases and abnormalities: general introduction]

La Prevention Des 13-Thalassemies En Belgique Francophone. II. Proposition D'Une Strategie.

Acta clinica Belgica·2016

Enzyme immunoassay screening of alpha 1-antitrypsin in dried blood spots from 39 289 newborns.

Clinical chemistry·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

Further delineation of a syndrome of cerebellar vermis hypo/aplasia, oligophrenia, congenital ataxia, coloboma, and hepatic fibrosis.

American journal of medical genetics·1989

[The prevention of beta-thalassemia in French-speaking Belgium. II. Proposal of a strategy].

Acta clinica Belgica·1989

[Prevention of beta-thalassemia in the French speaking part of Belgium. I. Epidemiologic, clinical, psycho-social and economic justifications].

Acta clinica Belgica·1989

[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

[Genetic and functional characterization of a novel KIT splicing variant in a Chinese three-generation pedigree with piebaldism].

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences·2026

Genome-wide association study of sarcopenia index reveals sex-stratified genetic architecture.

Biology of sex differences·2026

Whole-Exome Sequencing in a Consanguinity-Enriched South Indian Retinitis Pigmentosa Cohort: Diagnostic Yield and Molecular Spectrum.

Ophthalmology science·2026

Genetic analysis, reproductive decision-making, and pregnancy outcomes in 51 Chinese osteogenesis imperfecta families.

Journal of assisted reproduction and genetics·2026

Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

American journal of human genetics·2026

Natural variation in SL6 determines fatty acid components and seed longevity in rice.

Science advances·2026

Related Experiment Videos

[Prenatal diagnosis of hereditary diseases and abnormalities: general introduction]

Related Concept Videos

La Prevention Des 13-Thalassemies En Belgique Francophone. II. Proposition D'Une Strategie.

Enzyme immunoassay screening of alpha 1-antitrypsin in dried blood spots from 39 289 newborns.

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

Further delineation of a syndrome of cerebellar vermis hypo/aplasia, oligophrenia, congenital ataxia, coloboma, and hepatic fibrosis.

[The prevention of beta-thalassemia in French-speaking Belgium. II. Proposal of a strategy].

[Prevention of beta-thalassemia in the French speaking part of Belgium. I. Epidemiologic, clinical, psycho-social and economic justifications].

[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].

[Genetic and functional characterization of a novel KIT splicing variant in a Chinese three-generation pedigree with piebaldism].

Genome-wide association study of sarcopenia index reveals sex-stratified genetic architecture.

Whole-Exome Sequencing in a Consanguinity-Enriched South Indian Retinitis Pigmentosa Cohort: Diagnostic Yield and Molecular Spectrum.

Genetic analysis, reproductive decision-making, and pregnancy outcomes in 51 Chinese osteogenesis imperfecta families.

Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

Natural variation in SL6 determines fatty acid components and seed longevity in rice.

Related Experiment Videos

[Prenatal diagnosis of hereditary diseases and abnormalities: general introduction]

Related Concept Videos

Related Articles