BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

278 related articles for article (PubMed ID: 2865673)

  • 21. Tetrasomy 9p: an emerging syndrome.
    Jalal SM; Kukolich MK; Garcia M; Benjamin TR; Day DW
    Clin Genet; 1991 Jan; 39(1):60-4. PubMed ID: 1997218
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Cleft lip and palate, characteristic facial appearance, malrotation of the intestine, and lethal congenital heart disease in two sibs: a new autosomal recessive condition?
    McPherson E; Clemens M
    Am J Med Genet; 1996 Mar; 62(1):58-60. PubMed ID: 8779326
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 9p duplication confirmed by gene dosage effect: report of two patients.
    Zadeh TM; Funderburk SJ; Carrel R; Dumars KW
    Ann Genet; 1981; 24(4):242-4. PubMed ID: 6977307
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Phenotype of trisomy 9].
    Pfeiffer RA; Müller R
    Monatsschr Kinderheilkd; 1984 Oct; 132(10):797-800. PubMed ID: 6513939
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Duplication 3q: severe manifestations in an infant with duplication of a short segment of 3q.
    Rosenfeld W; Verma RS; Jhaveri RC; Estrada R; Evans H; Dosik H
    Am J Med Genet; 1981; 10(2):187-92. PubMed ID: 7315875
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Trisomy 16p in a liveborn infant and review of trisomy 16p.
    O'Connor TA; Higgins RR
    Am J Med Genet; 1992 Feb; 42(3):316-9. PubMed ID: 1536169
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
    Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Interstitial deletion of the short arm of chromosome 12. Report of a new patient and review of the literature.
    Fryns JP; Kleczkowska A; Van den Berghe H
    Ann Genet; 1990; 33(1):43-5. PubMed ID: 2195980
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies.
    Harrison KJ; Teshima IE; Silver MM; Jay V; Unger S; Robinson WP; James A; Levin A; Chitayat D
    Am J Med Genet; 1998 Sep; 79(2):103-7. PubMed ID: 9741467
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Eugenic counseling after a birth of an infant with congenital malformations].
    Beolchini PE
    Minerva Med; 1972 Nov; 63(85):4660-4. PubMed ID: 4264406
    [No Abstract]   [Full Text] [Related]  

  • 33. [Trisomy 9p - clinical and cytogenetic syndrome].
    Hitrec V; Zergollern L
    Acta Med Iugosl; 1979; 33(2):169-82. PubMed ID: 506795
    [No Abstract]   [Full Text] [Related]  

  • 34. 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; 111(1):76-80. PubMed ID: 12124740
    [TBL] [Abstract][Full Text] [Related]  

  • 35. New case of non-mosaic tetrasomy 9p in a severely polymalformed newborn girl.
    de Azevedo Moreira LM; Freitas LM; Gusmão FA; Riegel M
    Birth Defects Res A Clin Mol Teratol; 2003 Dec; 67(12):985-8. PubMed ID: 14745919
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Tetrasomy 9p: tissue-limited idic(9p) in a child with mild manifestations and a normal CVS result. Report and review.
    Grass FS; Parke JC; Kirkman HN; Christensen V; Roddey OF; Wade RV; Knutson C; Spence JE
    Am J Med Genet; 1993 Nov; 47(6):812-6. PubMed ID: 7506483
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Dermatoglyphics in children suffering from congenital defects, with and without chromosomal aberrations.
    Usoev SS
    Sov Genet; 1974 Jul; 8(7):929-31. PubMed ID: 4278489
    [No Abstract]   [Full Text] [Related]  

  • 38. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
    Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Analysis of banding patterns in a case of ring chromosome 21.
    Richer CL; Fitch N; Sitahal S; Murer-Orlando M; Jean P
    Am J Med Genet; 1981; 10(4):323-31. PubMed ID: 7332027
    [No Abstract]   [Full Text] [Related]  

  • 40. [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; 19(6):452-6. PubMed ID: 4089954
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.