[FAMILIAL TURNER'S SYNDROME. STUDY OF 2 FAMILIES WITH XO AND XX KARYOTYPES].
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Adolescent↗
Biomedical subjects
J FREZAL
Publications and source records attributed to J FREZAL.
[KLINEFELTER'S SYNDROME IN A HYPOSPADIC INFANT. KARYOTYPE WITH 46 CHROMOSOMES].
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Chromosomes↗
Congenital absence of beta-lipoproteins.
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Ataxia↗
[Chronic pneumopathy associated with an adenovirus infection].
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Adenoviridae Infections↗
[Diarrhea caused by disorders of the intestinal hydrolysis of saccharose, maltose and isomaltose].
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Diarrhea↗
[GENETIC ENCEPHALOPATHIES].
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Brain Diseases↗
[INTRODUCTION TO POPULATION GENETICS].
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Genetics, Medical↗
[CAUSES AND FREQUENCY OF CONGENITAL MALFORMATIONS].
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Abnormalities, Drug-Induced↗
[SERUM PROTEINS; PATHOLOGICAL CHANGES].
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Agammaglobulinemia↗
[SERUM PROTEINS AND ENZYMES (NORMAL VARIATIONS)].
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Blood Group Antigens↗
[STUDY OF A PAIR OF MONOZYGOTIC TWINS ONE OF WHOM WAS AFFLICTED WITH MYOPATHY (PSEUDO-HYPERTROPHIC FORM)].
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Child↗
[Various aspects of child pathology of genetic origin].
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Child↗
[Klinefelter's syndrome and hypospadias. Presence of 2 X chromosomes. Rupture of Y chromosome and translocation of its fragments].
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Chromosomes↗
[Inborn errors of lipid metabolism].
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Humans↗
[Congenital errors bearing on lipid metabolism].
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Child↗
[Galactosemia and the hereditary intolerance to fructose].
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Carbohydrate Metabolism↗
[Glycogenoses].
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Glycogen Storage Disease↗
[Hemolytic anemia caused by auto-antibodies].
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Anemia↗