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Journal Abstract Search

171 related items for PubMed ID: 2757362

  • 21. Proximal deletion of the long arm of chromosome 1: [del(1)(q23-q25)].
    Lo LJ, Noordhoff MS, Huang CS, Chen KT, Chen YR.
    Cleft Palate Craniofac J; 1993 Nov; 30(6):586-9. PubMed ID: 8280739
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  • 24. Interstitial deletion del(2)(q24q31) with a phenotype similar to del(2)(q31q33).
    Wamsler C, Müller B, Freyberger G, Schmid M.
    Am J Med Genet; 1991 May 01; 39(2):204-6. PubMed ID: 2063926
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  • 26. Congenital heart defect in a patient with deletion of chromosome 7q.
    Tiller GE, Watson MS, Duncan LM, Dowton SB.
    Am J Med Genet; 1988 Feb 01; 29(2):283-7. PubMed ID: 3354600
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  • 29. A 12 Mb deletion of 6p24.1-->pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys.
    Chen CP, Tzen CY, Chern SR, Tsai FJ, Hsu CY, Lee CC, Lee MS, Pan CW, Wang W.
    Eur J Med Genet; 2009 Feb 01; 52(1):59-61. PubMed ID: 19049908
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  • 30. Phenotypic variability in van der Woude syndrome.
    Lacombe D, Pedespan JM, Fontan D, Chateil JF, Verloes A.
    Genet Couns; 1995 Feb 01; 6(3):221-6. PubMed ID: 8588850
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  • 32. Gardner-Silengo-Wachtel or genito-palato-cadiac syndrome with associated autosomal aneuploidy.
    Golabi M, James AW, Desai N, Culver K, Cotter PD.
    Am J Med Genet A; 2009 Feb 15; 149A(4):693-7. PubMed ID: 19283856
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  • 33. Velo-cardio-facial and DiGeorge syndromes with meningomyelocele and deletions of the 22Q11 region.
    Nickel RE, Pillers DA, Merkens M, Magenis RE, Driscoll DA, Emanuel BS, Zonana J.
    Eur J Pediatr Surg; 1993 Dec 15; 3 Suppl 1():27-8. PubMed ID: 8130147
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  • 34. The 18q deletion syndrome and analysis of the critical region for orofacial cleft at 18q22.3.
    Dostal A, Nemeckova J, Gaillyova R.
    J Craniomaxillofac Surg; 2009 Jul 15; 37(5):272-5. PubMed ID: 19157891
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  • 35. Deletion of the proximal short arm of chromosome 8.
    Stratton RF, Crudo DF, Varela M, Shapira E.
    Am J Med Genet; 1992 Jan 01; 42(1):15-8. PubMed ID: 1308359
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  • 36. Del(4)(q33----qter): another case report of a child with mild dysmorphism.
    Fagan KA, Morris RB.
    J Med Genet; 1989 Dec 01; 26(12):776-8. PubMed ID: 2614797
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  • 37. A case of de novo translocation 7; 10 and the duplication 7p, deletion 10p phenotype.
    Park JP, McDermet MK, Moeschler JB, Wurster-Hill DH.
    Ann Genet; 1993 Dec 01; 36(4):217-20. PubMed ID: 8166428
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  • 38. Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.
    Stratton RF, Dobyns WB, Greenberg F, DeSana JB, Moore C, Fidone G, Runge GH, Feldman P, Sekhon GS, Pauli RM.
    Am J Med Genet; 1986 Jul 01; 24(3):421-32. PubMed ID: 3728561
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  • 39. The phenotypic and cytogenetic spectrum of partial trisomy 9.
    Wilson GN, Raj A, Baker D.
    Am J Med Genet; 1985 Feb 01; 20(2):277-82. PubMed ID: 3976721
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  • 40. Interstitial deletion for a region in the long arm of chromosome 16.
    Lin CC, Lowry RB, Snyder FF.
    Hum Genet; 1983 Feb 01; 65(2):134-8. PubMed ID: 6654327
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