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  • 1975-1979  (2)
  • 1965-1969  (1)
Material
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 22 (1966), S. 19-20 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Riassunto Nel plasma di neonati e di bambini in varie condizioni emolitiche è stata osservata una peculiare frazione proteica benzidino-positiva, elettroforeticamente più veloce dell'Hb libera. I risultati della casistica e di indagini sperimentali suggeriscono che questa frazione sia un prodotto di trasformazione dell'Hb (del tipo HbA3) e che nel plasma esistano sostanze non ultrafiltrabili capaci di accelerare la trasformazione a paragone di quanto si osserva nell'emolizzato. Queste sostanze sembrano più attive nei primi giorni di vita, specie nell'immaturo.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric radiology 5 (1977), S. 160-163 
    ISSN: 1432-1998
    Keywords: Urinary tract abnormalities ; Ureteral deformity ; Blind ureteric buds
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Four cases of blind ureteric bud are presented. This unusual abnormality is the result of abortive development of a normal bud or, more frequently, of an accessory bud brought into being by abnormal or premature division of the primary bud. — The disputed relationship between this abnormality and congenital ureteral and vescical diverticula is discussed. It is felt that the embryogenetic and anatomopathological evidence justifies the inclusion of some of the latter within the more extensive term “blind ureteric bud”.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Human genetics 〈Berlin〉 52 (1979), S. 69-77 
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A 49,XXXXX girl is reported. The most typical features of the patient are: severe mental retardation, serious dental anomalies, various anomalies of the bones, and a high rate of gonadotropins. The few similar cases so far described are reviewed to aid in delineation of this rare syndrome. The implications of Lyon's hypothesis on X-aneuploidies are also discussed.
    Type of Medium: Electronic Resource
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