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Journal Abstract Search

154 related items for PubMed ID: 6982665

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  • 4. Terminal (1)(q43) long-arm deletion of chromosome no. 1 in a three-year-old female.
    Mankinen CB, Sears JW, Alvarez VR.
    Birth Defects Orig Artic Ser; 1976; 12(5):131-6. PubMed ID: 953213
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  • 5. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
    Kobayashi J, Kimijima Y, Yamada S, Amagasa T, Saito-Ohara F.
    J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553
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  • 10. A case with 47,XXY,del(11)(q23) karotype-coexistence of Jacobsen and Klinefelter syndromes.
    Matheisel A, Babinska M, Wierzba J, Wozniak A, Nedoszytko B, Balcerska A, Limon J.
    Genet Couns; 2000 Jun; 11(3):267-71. PubMed ID: 11043435
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  • 11. Interstitial deletion 11q. Case report and review of the literature.
    De Pater JM, Ippel PF, Bijlsma JB, Van Nieuwenhuizen O.
    Genet Couns; 1997 Jun; 8(4):335-9. PubMed ID: 9457504
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  • 12. [Tetrasomy of the short arm of human chromosome 18: cytogenetics and phenotypic disorders].
    Kuleshov NP, Zaletaev DV, Levina LIa, Dement'eva GM, Arbuzov SP.
    Tsitol Genet; 1985 Jun; 19(6):452-6. PubMed ID: 4089954
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  • 13. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J, Plaza J, Geán E.
    An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149
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  • 14. Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:).
    Young RS, Palmer CG, Bender HA, Weaver DD, Hodes ME.
    Am J Med Genet; 1982 May; 12(1):103-7. PubMed ID: 7091193
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  • 15. [Partial deletion of the short arm of chromosome 4. Apropos of 3 cases].
    Taillemite JL, Tufferaud G, Hazael-Massieux P, Baheux-Morlier G, Roux C.
    Ann Genet; 1977 Jun; 20(2):93-100. PubMed ID: 302690
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  • 16. [Two new cases of partial monosomy 11q with breakpoint in 11q24 (author's transl)].
    Laurent C, Biemont MC, Veyron M, Guilhot J, Guibaud P.
    Ann Genet; 1979 Jun; 22(4):239-41. PubMed ID: 317789
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  • 17. A patient with partial duplication 2q and partial deficiency 11q.
    Ho CK, Henderson KC, Bowyer FP, Eilers KB, Andrews LG.
    Am J Med Genet; 1987 Nov; 28(3):575-9. PubMed ID: 3322008
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  • 18. Monosomy and trisomy of 15q24-qter with cleft lip and palate.
    Abe A, Hatano Y, Kurita K, Nakano M, Shimizu M, Yokoi T, Sugiyama N.
    Int J Oral Maxillofac Surg; 2008 May; 37(5):487-90. PubMed ID: 18262763
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  • 20. Mother and son with deletion of 3p25-pter.
    Tazelaar J, Roberson J, Van Dyke DL, Babu VR, Weiss L.
    Am J Med Genet; 1991 May 01; 39(2):130-2. PubMed ID: 2063913
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