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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

112 related items for PubMed ID: 1156680

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  • 3. [Congenital hydrocephalus, oligophrenia, dwarfism, centripetal obesity and hypogonadism; an X-linked recessive hereditary illness?].
    Sengers RC, Hamel BC, Otten BJ, van Gils JF, de Pagter AG.
    Tijdschr Kindergeneeskd; 1985 Feb; 53(1):31-4. PubMed ID: 4039476
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  • 4. Hypogonadotropic hypogonadism, mental retardation, obesity and minor skeletal abnormalities: another new autosomal recessive syndrome from the Middle East.
    Teebi AS, Al-Awadi SA, Farag TI, Naguib KK.
    Am J Med Genet; 1986 Jun; 24(2):373-8. PubMed ID: 3717216
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  • 9. Fibular hypoplasia and complex brachydactyly (Du Pan syndrome) in an inbred Pakistani kindred.
    Ahmad M, Abbas H, Wahab A, Haque S.
    Am J Med Genet; 1990 Jul; 36(3):292-6. PubMed ID: 2363425
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  • 12. Out-patient dietary management in the Prader-Willi syndrome.
    Coplin SS, Hine J, Gormican A.
    J Am Diet Assoc; 1976 Apr; 68(4):330-4. PubMed ID: 1254876
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  • 13. Brief clinical report: autosomal recessive anophthalmia with multiple congenital abnormalities--type Waardenburg.
    Richieri-Costa A, Gollop TR, Otto PG.
    Am J Med Genet; 1983 Apr; 14(4):607-15. PubMed ID: 6846395
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  • 14. [Willi-Prader-Labhardt's syndrome. Apropos of 2 cases].
    Bost M, Dieterlen M, Hadjian AJ, Joannard A, Jalbert P, Beaudoing A.
    Pediatrie; 1974 Apr; 29(3):291-6. PubMed ID: 4438036
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