[Early prenatal diagnosis in the framework of genetic counseling]

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

Whole-brain chemosensory responses of both C. elegans sexes.

Current biology : CB·2026

Clinical and functional characterization of 27 Chinese patients with 46, XY disorders of sex development caused by novel NR5A1 variants.

Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation·2026

Infantile Epileptic Spasms Syndrome Complicating Mosaic Down-Turner Syndrome: A Case Report.

Clinical case reports·2026

Sex-specific differences in pancreatic α-cell function.

Frontiers in endocrinology·2026

First Cornelia de Lange Syndrome Type 4 Caused by the Gonadal Mosaicism of RAD21 Deletion.

Human mutation·2026

The genome sequence of a caddisfly, Limnephilus rhombicus (Linnaeus, 1758).

Wellcome open research·2026

Related Experiment Videos

[Early prenatal diagnosis in the framework of genetic counseling]

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].

Whole-brain chemosensory responses of both C. elegans sexes.

Clinical and functional characterization of 27 Chinese patients with 46, XY disorders of sex development caused by novel NR5A1 variants.

Infantile Epileptic Spasms Syndrome Complicating Mosaic Down-Turner Syndrome: A Case Report.

Sex-specific differences in pancreatic α-cell function.

First Cornelia de Lange Syndrome Type 4 Caused by the Gonadal Mosaicism of RAD21 Deletion.

The genome sequence of a caddisfly, Limnephilus rhombicus (Linnaeus, 1758).

Related Experiment Videos

[Early prenatal diagnosis in the framework of genetic counseling]

Related Concept Videos

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