[Two familial cases of congenital erythroderma ichthyosiforme].
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Female↗
Biomedical subjects
C Lambotte
Publications and source records attributed to C Lambotte.
[Genetic counseling. I. Introduction. Definition and objectives].
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Chromosome Aberrations↗
[Galactokinase deficiency, cause of hereditary cataract. Recent publications].
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Adolescent↗
[Prenatal detection of embryofetal malformations through the analysis of amniotic fluid, especially determination of alpha 1-fetoprotein].
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Amniocentesis↗
[Etiology of anencephalus and spina bifida].
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Anencephaly↗
[Incidence of chromosome aberrations].
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Adult↗
[Genetic pathology in pediatrics].
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Belgium↗
[Value of neonatal diagnosis of phenylketonuria].
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Female↗
[Tumoral calcinosis, a hereditary disease of variable incidence].
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Black People↗
Letter: Sickle cell anemia and dietary precursors of cyanate.
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Adolescent↗
[Case of severe neonatal craniofacial dysostosis. Crouzon's syndrome with the aspect of "trefoil cranium"].
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Autopsy↗
Telomeric tandem translocation tan (14; 15) (q32; q26) and absence of IgA in an incestuous child.
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Abnormalities, Multiple↗
[Sickle-cell anemia in children in black Africa].
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Africa↗
[Neonatal diagnosis of hereditary metabolic diseases].
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Acidosis↗
[Treatment of mucopolysaccharidoses with perfusions of plasma or leukocytes].
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Blood Transfusion↗
[The Hallermann-Streiff-François syndrome or "bird head" dyscephaly].
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Abnormalities, Multiple↗
[Vital risk and malformative risk in children of diabetic mothers].
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Congenital Abnormalities↗