[TRISOMY 18. 5 NEW CASES. REVIEW OF THE LITERATURE].
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Chromosomes, Human, Pair 18↗
Biomedical subjects
J LAFOURCADE
Publications and source records attributed to J LAFOURCADE.
[ERYTHEMA MULTIFORME AND REOVIRUS INFECTION].
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Animals↗
[HISTIOCYTIC GRANULOMATOUS DISEASE (HISTIOCYTOSIS X). APROPOS OF 2 CASES].
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Child↗
[A FAMILIAL DISEASE PRESENTING IN CERTAIN SUBJECTS THE APPEARANCE OF EULENBURG'S PARAMYOTONIA AND RESEMBLING IN OTHERS HEREDITARY EPISODIC ADYNAMIA].
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Acetazolamide↗
[PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME].
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Chromosome Aberrations↗
[FAMILIAL SEGREGATION OF A 5-13 TRANSLOCATION DETERMINING PARTIAL MONOSOMY AND A TRISOMY OF THE SHORT ARM OF THE 5 CHROMOSOME: "CAT CRY" DISEASE AND ITS "RECEPROCAL"].
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Arm↗
[PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 5. INDIVIDUALIZATION OF A NEW MORBID STATE].
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Arm↗
[PECULIARITIES OF WATER AND ELECTROLYTE METABOLISM IN THE INFANT; PHYSIOPATHOLOGY OF ACUTE DEHYDRATION].
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Acid-Base Equilibrium↗
[CLINICAL AND BIOLOGICAL EXAMINATION OF AN ACUTE DEHYDRATION (DURING THE INITIAL PERIOD)].
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Anuria↗
[IMMEDIATE PROGNOSIS OF ACUTE DEHYDRATION. SUBSEQUENT PROGNOSIS AND FUTURE OF THESE CHILDREN].
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Child↗
[PARTIAL DELETION OF THE SHORT ARM OF THE 5 CHROMOSOME: THE 5TH CASE OF CRYING CAT SYNDROME].
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Arm↗
[3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME].
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Arm↗
[Wilson's disease with preceding hepatic and hematological symptoms in a 10-year-old child].
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Anemia↗
[FAMILIAL 2 - 22 TRANSLOCATION; ASSOCIATION WITH A HAPLO-X TURNER'S SYNDROME].
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Blood Group Antigens↗
[Heterokaryotic monozygotism, normal twin and 21 trisomal twin].
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Chromosomes↗
[Thalassodepranocytic disease. Genetic and biological study of a case].
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Anemia↗
[Presumption of monozygotism in spite of a sexual dimorphism: XY male subject and haploid X neuter subject].
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Chromosomes↗
[The genetic determinism of sex].
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Chromosomes↗