[Prenatal diagnosis of genetic disorders]

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

QTL mapping.

Genetics·2026

Genetic Insights Into Retinitis Pigmentosa: A De Novo RPGR Mutation in an Iranian-Azeri Family.

Case reports in ophthalmological medicine·2026

Altered thalamo-prefrontal synchrony dynamics during spatial working memory task performance in a SETD1A loss-of-function mouse model of schizophrenia predisposition.

Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology·2026

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Regenerative therapy·2026

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Italian journal of pediatrics·2026

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Diabetes·2026

Related Experiment Videos

[Prenatal diagnosis of genetic disorders]

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].

QTL mapping.

Genetic Insights Into Retinitis Pigmentosa: A De Novo RPGR Mutation in an Iranian-Azeri Family.

Altered thalamo-prefrontal synchrony dynamics during spatial working memory task performance in a SETD1A loss-of-function mouse model of schizophrenia predisposition.

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Related Experiment Videos

[Prenatal diagnosis of genetic disorders]

Related Concept Videos

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