Biomedical subjects

L GEDDA

Publications and source records attributed to L GEDDA.

At least 19 recordsLinked to original sources

PubMed1965

[CONTRIBUTION OF THE CLINICO-TWIN METHOD IN STUDY OF SEX ANOMALIES IN CHILDHOOD. (CASES OF TWINS WITH PHIMOSIS, HYPOSPADIAS, CRYPTORCHISM, HYPOPITUITARISM, ADIPOSO-GENITAL SYNDROME AND THE LAURENCE-MOON-BIEDL TYPE SYNDROME)].

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Adolescent↗

PubMed1965

[GENETIC AND IMMUNOLOGIC PROBLEMS OF ORGAN TRANSPLANTS].

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Genetic Therapy↗

PubMed1965

HUMAN MONOZYGOTIC AND PLURIZYGOTIC MULTIPLE BIRTHS: HEREDITY AND HORMONE ACTION.

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Female↗

PubMed1965

[APPLICATION OF GENETICS TO MEDICAL PRACTICE. (THE HUMAN CONSTITUTION FROM THE GENETIC VIEWPOINT--THE "CHRONON" CONCEPT AND ITS APPLICATION TO MEDICINE)].

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Body Constitution↗

PubMed1964

THE CONTRIBUTION OF THE "CLINICAL TWIN METHOD" TO THE STUDY OF SEX ANOMALIES IN CHILDHOOD.

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Adolescent↗

PubMed1964

ARE VITAL TWINS PREMATURES?

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Humans↗

PubMed1964

[STUDY OF NORMAL BLOOD COAGULATION IN TWINS WITH THE THROMBELASTOGRAPHIC METHOD].

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Adolescent↗

PubMed1964

[TAGE KEMP. AUG. 28, 1896-JAN. 7-1964].

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Genetics, Medical↗

PubMed1964

[RESEARCH ON HUMAN CHROMOSOMES WITH THE TWIN TEST. (I. DETERMINATION OF THE MITOTIC INDEX IN MONOZYGOTIC AND DIZYGOTIC PAIRS)].

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Cell Division↗

PubMed1964

[THE COMPLEX CONTRIBUTION OF GENOTYPE TO MORBID PREDISPOSITION. (THE ROLE OF PREDISPOSITION IN TUBERCULOSIS, SILICOSIS AND ALLERGIC DISEASES)].

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Asthma↗

PubMed1963

ON THE STATISTICAL SIGNIFICANCE OF ONE PAIR OF MONOZYGOTIC TWINS IN CLINICAL GENETICS.

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Biometry↗

PubMed1963

[Aseptic gangrene of the cranium as hereditary circumscribed aplasia of the newborn].

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Bone and Bones↗

PubMed1963

[The problem of the ovular adnexa in twin pregnancies].

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Female↗

PubMed1963

[GENETIC ASPECTS OF HOMOSEXUALITY].

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Disorders of Sex Development↗

PubMed1963

[SUBTOTAL APLASIA OF THE UPPER EXTREMITIES IN A DISCORDANT MONOZYGOTIC TWIN PAIR].

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Arm↗

PubMed1962

The genetic aspects of anaesthesiology.

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Anesthesia↗

PubMed1962

[Proposed azygotic twin test].

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Humans↗

PubMed1962

[Cases of familial Werdnig-Hoffmann syndrome, including a pair of concordant monozygotic twins (a case from the Eugenic Consultation Clinic)].

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Disease↗