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Journal Abstract Search

188 related items for PubMed ID: 2130760

  • 1. [Prader-Willi-Labhart syndrome: relations with the hypothalamus and chromosome 15].
    Touraine P, Mbikay M, Seidah NG, Chrétien M.
    Ann Endocrinol (Paris); 1990; 51(5-6):202-8. PubMed ID: 2130760
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  • 2. [Chromosome aberrations in Prader-Willi-Labhart syndrome--critical review, documented by 4 unusual cases].
    Pfeiffer RA, Tschech L, Irle U, Wündisch GF.
    Klin Padiatr; 1987; 199(5):329-35. PubMed ID: 3316824
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  • 3. [Self-induced cutaneous lesions in Prader-Willi syndrome].
    Plantin P, Milochau P, Broussine L, Blondin G.
    Ann Dermatol Venereol; 1997; 124(5):390-2. PubMed ID: 9739896
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  • 5. Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population.
    Cassidy SB, Thuline HC, Holm VA.
    Am J Med Genet; 1984 Feb; 17(2):485-95. PubMed ID: 6336316
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  • 7. [Molecular analysis in Prader-Willi syndrome diagnosis].
    Szpecht-Potocka A.
    Med Wieku Rozwoj; 1999 Feb; 3(3):407-19. PubMed ID: 10910667
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  • 8. Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.
    Gilhuis HJ, van Ravenswaaij CM, Hamel BJ, Gabreëls FJ.
    Eur J Paediatr Neurol; 2000 Feb; 4(1):39-43. PubMed ID: 10701104
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  • 12. Neonatal presentation of Prader Willi sindrome. Personal records.
    Maggio MC, Corsello M, Piccione M, Piro E, Giuffrè M, Liotta A.
    Minerva Pediatr; 2007 Dec; 59(6):817-23. PubMed ID: 17978792
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  • 14. Molecular genetic analysis of the Prader-Willi syndrome by using fluorescent multiplex PCR of the dinucleotide repeats on chromosome 15q11-q13.
    Lee MJ, Nishio H, Nagai T, Okamoto N, Yuki T, Sumino K.
    Clin Chim Acta; 1998 Mar 09; 271(1):89-96. PubMed ID: 9564560
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  • 20. Prader-Willi syndrome.
    Cassidy SB, Ledbetter DH.
    Neurol Clin; 1989 Feb 09; 7(1):37-54. PubMed ID: 2646521
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