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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

365 related items for PubMed ID: 47396

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  • 3. Duplication 11p11.3 leads to 14.1 to meiotic crossing--over.
    Strobel RJ, Riccardi VM, Ledbetter DH, Hittner HM.
    Am J Med Genet; 1980; 7(1):15-20. PubMed ID: 7211949
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  • 6. A new case of the trisomy 9P syndrome. Report of a patient with unusual chromosome findings (46,XX/47,XX, + i (9p) and a peculiar congenital heart defect.
    Orye E, Verhaaren H, Van Egmond H, Devloo-Blancquaert A.
    Clin Genet; 1975 Feb; 7(2):134-43. PubMed ID: 1132161
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  • 7. Genetics of the Meckel syndrome (dysencephalia splanchnocystica).
    Hsia YE, Bratu M, Herbordt A.
    Pediatrics; 1971 Aug; 48(2):237-47. PubMed ID: 4997860
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  • 9. The dup(3q) syndrome: report of eight cases and review of the literature.
    Steinbach P, Adkins WN, Caspar H, Dumars KW, Gebauer J, Gilbert EF, Grimm T, Habedank M, Hansmann I, Herrmann J, Kaveggia EG, Langenbeck U, Meisner LF, Najafzadeh TM, Opitz JM, Palmer CG, Peters HH, Scholz W, Tavares AS, Wiedeking C.
    Am J Med Genet; 1981 Aug; 10(2):159-77. PubMed ID: 7315873
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  • 11. Deletion from the long arm of chromosome 4 (46,XX,4q-) associated with congenital anomalies.
    Golbus MS, Conte FA, Daentl DL.
    J Med Genet; 1973 Mar; 10(1):83-5. PubMed ID: 4121427
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  • 12. 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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  • 14. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
    Jacobsen P, Hauge M, Henningsen K, Hobolth N, Mikkelsen M, Philip J.
    Hum Hered; 1973 Jun; 23(6):568-85. PubMed ID: 4134631
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  • 17. [Van der Woude syndrome in combination with ring chromosome 18].
    Kalker U, Gabriel M, Jacobi G.
    Monatsschr Kinderheilkd; 1988 Feb; 136(2):95-8. PubMed ID: 3367915
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  • 18. Heart disease associated with deletion of the short arm of chromosome 18.
    Movahhedian HR, Kane HA, Borgaonkar D, McDermott M, Septimus S.
    Del Med J; 1991 May; 63(5):285-9. PubMed ID: 1860515
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  • 19. Two chromosomal syndromes in the same family: monosomy and trisomy for part of the short arm of chromosome 10.
    Slinde S, Hansteen IL.
    Eur J Pediatr; 1982 Oct; 139(2):153-7. PubMed ID: 7151837
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  • 20. [Holt-Oram syndrome with chromosomopathy (author's transl)].
    González Espinosa C, Artiles Pérez L, García Báez M, Otero Gómez A, García Miranda JL.
    An Esp Pediatr; 1982 Jan; 16(1):77-81. PubMed ID: 7081854
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