These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 6800299)

  • 41. [Partial deletion of the short arm of the chromosome 9].
    Serville F; Allain D; Broustet A; Martin C; Gachet M; Babin JP; Cenraud J
    Ann Genet; 1976 Jun; 19(2):143. PubMed ID: 1085605
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Comparative pathology of trisomies D and E].
    Bocquet L
    Union Med Can; 1968 Jul; 97(7):907-23. PubMed ID: 5709533
    [No Abstract]   [Full Text] [Related]  

  • 43. Interstitial deletion of 11q.
    Guć-Sćekić M; Pilić-Radivojević G; Mrdjenović G; Djurić M
    J Med Genet; 1989 Mar; 26(3):205-6. PubMed ID: 2468775
    [No Abstract]   [Full Text] [Related]  

  • 44. [Wolf syndrome. Apropos of 2 cases].
    García González P; Pedraz García C; Merino Marcos L; Salazar Veloz J; Escudero Bueno G; Salazar Villalobos V
    An Esp Pediatr; 1983 Feb; 18(2):113-7. PubMed ID: 6881733
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Interstitial deletion and ring chromosome derived from 16q.
    Krauss CM; Caldwell D; Atkins L
    J Med Genet; 1987 May; 24(5):308-12. PubMed ID: 3585948
    [TBL] [Abstract][Full Text] [Related]  

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

  • 47. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J; Plaza J; Geán E
    An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q.
    Cousineau AJ; Higgins JV; Scott-Emuakpor AB; Mody G
    Am J Med Genet; 1983 Jan; 14(1):29-35. PubMed ID: 6829609
    [TBL] [Abstract][Full Text] [Related]  

  • 49. De novo partial 2p duplication with postmortem description.
    Monteleone PL; Blair JD; Graviss ER; Chen SC; Salvador A; Grzegocki JA; Monteleone JA
    Am J Med Genet; 1981; 10(1):55-64. PubMed ID: 7197468
    [TBL] [Abstract][Full Text] [Related]  

  • 50. 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]  

  • 51. 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]  

  • 52. 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]  

  • 53. Monosomy 11q: report of two familial cases and review of the literature.
    Hustinx R; Verloes A; Grattagliano B; Herens C; Jamar M; Soyeur D; Schaaps JP; Koulischer L
    Am J Med Genet; 1993 Sep; 47(3):312-7. PubMed ID: 8135272
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Triploidy syndrome and diploid/triploid mixoploidy syndrome].
    Kato R
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):361-2. PubMed ID: 11057261
    [No Abstract]   [Full Text] [Related]  

  • 55. Mother to son transmission of del(1) (q42.1q42.3).
    Sanford Hanna JA; Ball S; Pagon RA; Donlan M
    Am J Med Genet; 2001 Jan; 98(1):103-6. PubMed ID: 11426447
    [TBL] [Abstract][Full Text] [Related]  

  • 56. del(20p) with manifestations of arteriohepatic dysplasia.
    Byrne JL; Harrod MJ; Friedman JM; Howard-Peebles PN
    Am J Med Genet; 1986 Aug; 24(4):673-8. PubMed ID: 3740100
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Del(14)(q22.1q23.2) in a patient with anophthalmia and pituitary hypoplasia.
    Lemyre E; Lemieux N; Décarie JC; Lambert M
    Am J Med Genet; 1998 May; 77(2):162-5. PubMed ID: 9605291
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Interstitial deletion 6q in a malformed boy.
    Nakagome Y; Tanaka T; Hashimoto T; Kuyama M; Maruyama M
    Ann Genet; 1980; 23(1):49-51. PubMed ID: 6965841
    [No Abstract]   [Full Text] [Related]  

  • 59. Loss of the N-myc oncogene in a patient with a small interstitial deletion of the short arm of chromosome 2.
    Saal HM; King LJ; Zimmerman D; Johnson RC; Carr AG; Samango-Sprouse CA; Stanley W
    Am J Med Genet; 1996 Dec; 66(4):373-7. PubMed ID: 8989454
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [A new case of ring chromosome 9].
    Portnoi MF; van den Akker J; Le Porrier N; Joye N; Youssef S; Taillemite JL
    Sem Hop; 1983 Jan; 59(3):185-8. PubMed ID: 6301043
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.