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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

196 related items for PubMed ID: 6360648

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  • 3. [Mass screening of the hereditary abnormalities in the pupils of the elementary schools in Milan].
    Morganti G.
    Minerva Med; 1972 Nov 28; 63(85):4641-3. PubMed ID: 4639981
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  • 4. [Clinical and chromosomal studies in a congenital hypothyroidism caused by thyroxin synthesis disorders and middle ear hearing disorders (Pendred- or goiter-deafness syndrome)].
    Kitlak W, Gebert P.
    Arch Kinderheilkd; 1968 Nov 28; 177(2):170-83. PubMed ID: 5723894
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  • 6. Syndromes and systemic diseases with eye findings.
    Sargent RA.
    Pediatrician; 1990 Nov 28; 17(3):183-93. PubMed ID: 2194183
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  • 7. Heredity hearing losses with delayed onset: mechanisms of expression.
    Jahn AF, Noyek AM.
    Otolaryngol Clin North Am; 1981 Feb 28; 14(1):59-64. PubMed ID: 6789283
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  • 12. Disabilities of genetic origin.
    Sterling HM.
    Arch Phys Med Rehabil; 1970 May 28; 51(5):291-6 passim. PubMed ID: 4246188
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  • 13. [Genetics in eye diseases].
    Keith CG.
    Buch Augenarzt; 1981 May 28; (83):1-127. PubMed ID: 6784888
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  • 15. Genetic aspects of renal disease: a survey of the various recognized forms.
    Platt M.
    Clin Pediatr (Phila); 1976 Nov 28; 15(11):1024-8. PubMed ID: 184999
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  • 16. [Childhood obesity as a symptom of genetic syndromes].
    Seemanová E, Rüdiger HW, Dreyer M.
    Cesk Pediatr; 1989 May 28; 44(5):268-74. PubMed ID: 2752454
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  • 18. [A new autosomal-recessive hereditary syndrome. Multiple peripheral pulmonary stenosis, brachytelephalangia, inner-ear deafness, ossification or calcification of cartilages].
    Keutel J, Jörgensen G, Gabriel P.
    Dtsch Med Wochenschr; 1971 Oct 22; 96(43):1676-81 passim. PubMed ID: 5099199
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