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Journal Abstract Search

149 related items for PubMed ID: 3209683

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Further delineation of pseudotrisomy 13 syndrome: a case without polydactyly.
    Ramos-Arroyo MA, de Miguel C, Valiente A, Moreno-Laguna S.
    Am J Med Genet; 1994 Apr 01; 50(2):177-9. PubMed ID: 8010349
    [Abstract] [Full Text] [Related]

  • 23. [Severe pre-eclampsia and fetal trisomy 13 in a multiparous woman].
    Pedersen BW, Grønlund A.
    Ugeskr Laeger; 2003 May 12; 165(20):2108-9. PubMed ID: 12812105
    [Abstract] [Full Text] [Related]

  • 24. [Syndrome of congenital malformations and dysmorphic features in a newborn with partial trisomy 16q due to maternal translocation t(9;16)(p24;q13)].
    Luberda-Zapaśnik J, Midro AT, Szwałkiewicz-Warowicka E.
    Pediatr Pol; 1995 Sep 12; 70(9):769-73. PubMed ID: 8657511
    [Abstract] [Full Text] [Related]

  • 25. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS, Kamel AK, Helmy NA.
    Genet Couns; 2008 Sep 12; 19(2):199-209. PubMed ID: 18618995
    [Abstract] [Full Text] [Related]

  • 26. [Trisomy 13 syndrome, Patau syndrome].
    Tsukino R, Sasaki M.
    Ryoikibetsu Shokogun Shirizu; 2000 Sep 12; (30 Pt 5):332-4. PubMed ID: 11057250
    [No Abstract] [Full Text] [Related]

  • 27. Plurimalformative syndrome associating trisomy 18 and omphalocele. Case report and review of the literature.
    Ţarcă E, Plămădeală P, Savu B.
    Rom J Morphol Embryol; 2014 Sep 12; 55(1):209-13. PubMed ID: 24715190
    [Abstract] [Full Text] [Related]

  • 28. [Malformations in otorhinolaryngology. Genetic report].
    Jörgensen G.
    Arch Klin Exp Ohren Nasen Kehlkopfheilkd; 1972 Sep 12; 202(2):253-62. PubMed ID: 4264984
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. Double trisomy (48,XXX, +18).
    Tsukahara M, Fukuda M, Furukawa S, Kondoh O.
    Am J Med Genet; 1994 Aug 15; 52(2):244. PubMed ID: 7802021
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Isochromosome (18q) in siblings.
    Krüger G, Götz J, Dunker H, Pelz L.
    Clin Genet; 1987 Oct 15; 32(4):249-53. PubMed ID: 3677464
    [Abstract] [Full Text] [Related]

  • 33. Multiple congenital malformations in two sibs reminiscent of hydrolethalus and pseudotrisomy 13 syndromes.
    Dincsoy MY, Salih MA, al-Jurayyan N, al Saadi M, Patel PJ.
    Am J Med Genet; 1995 Apr 10; 56(3):317-21. PubMed ID: 7778599
    [Abstract] [Full Text] [Related]

  • 34. Frequency of chromosomal aberrations in newborn infants with multiple developmental defects.
    Chebotarev AN.
    Sov Genet; 1974 Sep 15; 8(10):1329-30. PubMed ID: 4439048
    [No Abstract] [Full Text] [Related]

  • 35. [Trisomy 18 syndrome(Edwards syndrome)].
    Ieshima A.
    Ryoikibetsu Shokogun Shirizu; 2000 Sep 15; (30 Pt 5):340-1. PubMed ID: 11057253
    [No Abstract] [Full Text] [Related]

  • 36. Distal partial trisomy 1q: report of two cases and a review of the literature.
    Utine GE, Aktas D, Alanay Y, Gücer S, Tuncbilek E, Mrasek K, Liehr T.
    Prenat Diagn; 2007 Sep 15; 27(9):865-71. PubMed ID: 17605151
    [Abstract] [Full Text] [Related]

  • 37. [20 cases of trisomy 18. Sex-ratio in relation to age of the mother].
    Le Marec BM, Lair JC, Kérisit J, Le Mée F, Sénécal J.
    Ann Pediatr (Paris); 1977 Feb 15; 24(2):125-36. PubMed ID: 16211953
    [No Abstract] [Full Text] [Related]

  • 38. [Management of severe ear aplasias].
    Manach Y.
    Acta Otorhinolaryngol Belg; 1987 Feb 15; 41(4):564-73. PubMed ID: 3425296
    [Abstract] [Full Text] [Related]

  • 39. An infant with double trisomy (48,XXX, + 18).
    Jaruratanasirikul S, Jinorose U.
    Am J Med Genet; 1994 Jan 15; 49(2):207-10. PubMed ID: 8116670
    [Abstract] [Full Text] [Related]

  • 40. Patau syndrome with long survival in a case of unusual mosaic trisomy 13.
    Fogu G, Maserati E, Cambosu F, Moro MA, Poddie F, Soro G, Bandiera P, Serra G, Tusacciu G, Sanna G, Mazzarello V, Montella A.
    Eur J Med Genet; 2008 Jan 15; 51(4):303-14. PubMed ID: 18495567
    [Abstract] [Full Text] [Related]

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