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Journal Abstract Search

442 related items for PubMed ID: 6539070

  • 21. Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two cases.
    Schimmenti LA, Higgins RR, Mendelsohn NJ, Casey TM, Steinberger J, Mammel MC, Wiesner GL.
    Am J Med Genet; 1995 May 22; 57(1):52-6. PubMed ID: 7645598
    [Abstract] [Full Text] [Related]

  • 22. Trisomy 18 with unilateral atypical ectrodactyly.
    Rogers RC.
    Am J Med Genet; 1994 Jan 01; 49(1):125-7. PubMed ID: 8172239
    [No Abstract] [Full Text] [Related]

  • 23. Duplication of (2)(q11.1-q13.2) in a boy with mental retardation and cleft lip and palate: another clefting gene locus on proximal 2q?
    Riegel M, Schinzel A.
    Am J Med Genet; 2002 Jul 22; 111(1):76-80. PubMed ID: 12124740
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  • 24. Walker-Warburg syndrome with cleft lip and cleft palate in two sibs.
    Burton BK, Dillard RG, Weaver RG.
    Am J Med Genet; 1987 Jul 22; 27(3):537-41. PubMed ID: 3631127
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  • 25. Deletion of the short arm of chromosome No. 10.
    Shokeir MH, Ray M, Hamerton JL, Bauder F, O'Brien H.
    J Med Genet; 1975 Mar 22; 12(1):99-103. PubMed ID: 47396
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  • 26. De novo partial duplications 1p: report of two new cases and review.
    Garcia-Heras J, Corley N, Garcia MF, Kukolich MK, Smith KG, Day DW.
    Am J Med Genet; 1999 Jan 29; 82(3):261-4. PubMed ID: 10215552
    [Abstract] [Full Text] [Related]

  • 27. De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.
    Legare JM, Sekhon GS, Laxova R.
    Am J Med Genet; 1994 Nov 15; 53(3):216-21. PubMed ID: 7856655
    [Abstract] [Full Text] [Related]

  • 28. Trisomy chromosome (22)(q13.1-qter) as a result of paternal inversion (22)(p11q13.1) proved using region-specific FISH probes.
    Hou JW.
    Chang Gung Med J; 2005 Sep 15; 28(9):657-61. PubMed ID: 16323558
    [Abstract] [Full Text] [Related]

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  • 30. Molecular cytogenetic analysis of de novo dup(5)(q33.1q31.1) associated with abnormal perinatal findings.
    Chen CP, Lin SP, Chern SR, Lin CC, Li YC, Lee CC, Hsieh LJ, Chen WL, Wang W.
    Prenat Diagn; 2006 Feb 15; 26(2):181-3. PubMed ID: 16470511
    [No Abstract] [Full Text] [Related]

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  • 32. [Cardiac symptoms in 2 patients with Seckel syndrome].
    Rappen U, von Brenndorff AI.
    Monatsschr Kinderheilkd; 1993 Jul 15; 141(7):584-6. PubMed ID: 8413337
    [Abstract] [Full Text] [Related]

  • 33. Dir dup(X) (q13-->qter) in a girl with growth retardation, microcephaly, developmental delay, seizures, and minor anomalies.
    Aughton DJ, AlSaadi AA, Johnson JA, Transue DJ, Trock GL.
    Am J Med Genet; 1993 Apr 15; 46(2):159-64. PubMed ID: 7683452
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  • 37. Trisomy 22 confirmed by fluorescent in situ hybridization.
    Stratton RF, DuPont BR, Mattern VL, Young RS, McCourt JW, Moore CM.
    Am J Med Genet; 1993 Apr 01; 46(1):109-12. PubMed ID: 8494030
    [Abstract] [Full Text] [Related]

  • 38. 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 01; 28(3):165-70. PubMed ID: 10964553
    [Abstract] [Full Text] [Related]

  • 39. De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay.
    Chen CP, Lin SP, Chern SR, Lee CC, Huang JK, Wang W, Liao YW.
    Genet Couns; 2004 Jun 01; 15(4):437-42. PubMed ID: 15658619
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