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 *

99 related articles for article (PubMed ID: 691837)

  • 1. A partial short arm deletion of chromosome 20:46, XY, del(20)(p11).
    Kogame K; Fukuhara T; Maeda A; Kudo Y
    Jinrui Idengaku Zasshi; 1978 Jun; 23(2):153-60. PubMed ID: 691837
    [No Abstract]   [Full Text] [Related]  

  • 2. [Partial monosomy 20q : a new syndrome. Regional assignment of the ADA locus on 20q132 (author's transl)].
    Fraisse J; Bertheas MF; Frère F; Lauras B; Rolland MO; Brizard CP
    Sem Hop; 1982 Jun; 58(22):1366-9. PubMed ID: 6287596
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5.
    Keppen LD; Gollin SM; Edwards D; Sawyer J; Wilson W; Overhauser J
    Am J Med Genet; 1992 Oct; 44(3):356-60. PubMed ID: 1488985
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20.
    Okada M; Usami A; Okajima K; Yamada M; Yamaguchi Y; Umezaki I; Matsuda Y; Ohta H
    Congenit Anom (Kyoto); 2005 Dec; 45(4):161-4. PubMed ID: 16359498
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Terminal deletion of the short arm of chromosome 3.
    Asai M; Ito Y; Iguchi T; Ito J; Okada N; Oishi H
    Jpn J Hum Genet; 1992 Jun; 37(2):163-8. PubMed ID: 1391972
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Alagille syndrome (arteriohepatic dysplasia) and del(20)(p11.2).
    Legius E; Fryns JP; Eyskens B; Eggermont E; Desmet V; de Bethune G; Van den Berghe H
    Am J Med Genet; 1990 Apr; 35(4):532-5. PubMed ID: 2333885
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)].
    Chitayat D; Babul R; Silver MM; Jay V; Teshima IE; Babyn P; Becker LE
    Am J Med Genet; 1996 Jan; 61(1):45-8. PubMed ID: 8741917
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Occurrence of 19p- in an infant with multiple dysmorphic features.
    Hurgoiu V; Suciu S
    Ann Genet; 1984; 27(1):56-7. PubMed ID: 6609675
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Deletion of the long arm of the first chromosome pair in a 3-year-old boy, 46 XY DEL (1) (q43)].
    Michałowicz-Wojczyńska E; Migdalska M; Swiatkowska E
    Pediatr Pol; 1985 Sep; 60(9):662-6. PubMed ID: 3831900
    [No Abstract]   [Full Text] [Related]  

  • 10. Interstitial deletion of the short arm of chromosome 8: report of a patient and review of the literature.
    Plomp AS; Schrander-Stumpel CT; Engelen JJ; Sijstermans JM; Loneus WH; Fryns JP
    Genet Couns; 1995; 6(1):55-60. PubMed ID: 7794563
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interstitial deletion of the short arm of chromosome 4. A phenotype distinct from the Wolf-Hirschhorn syndrome.
    Fryns JP; Yang-Aisheng ; Kleczkowska A; Lemmens F; Vandecasseye W; van den Berghe H
    Ann Genet; 1989; 32(1):59-61. PubMed ID: 2751251
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Partial deletion of the short arm of chromosome 12(p11; p13). Report of a case.
    Tenconi R; Baccichetti C; Anglani F; Pellergrino PA; Kaplan JC; Junien C
    Ann Genet; 1975 Jun; 18(2):95-8. PubMed ID: 1081371
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial trisomy 20 confirmed by gene dosage studies.
    Rudd NL; Bain HW; Giblett E; Chen SH; Worton RG
    Am J Med Genet; 1979; 4(4):357-64. PubMed ID: 231907
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 7q deletion syndrome (7q32 leads to 7qter).
    Harris EL; Wappner RS; Palmer CG; Hall B; Dinno N; Seashore MR; Breg WR
    Clin Genet; 1977 Oct; 12(4):233-8. PubMed ID: 912940
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].
    Wilson MG; Towner JW; Forsman I; Siris E
    Am J Med Genet; 1979; 3(2):155-74. PubMed ID: 474629
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deletion of a portion of the long arm of chromosome 6.
    Goldberg R; Fish B; Ship A; Shprintzen RJ
    Am J Med Genet; 1980; 5(1):73-80. PubMed ID: 7395903
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A case of interstitial 1q deletion [46,XY,del(q25q32.1)].
    Hamano S; Fukushima Y; Yamada T; Shimizu H; Okuyama M; Ito F; Maekawa K
    Ann Genet; 1987; 30(2):105-8. PubMed ID: 3314663
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Thrombocytopenia and cleft hand in monosomy 21.
    Vogels A; de Smet L; van den Berghe H; Fryns JP
    Genet Couns; 1994; 5(1):67-71. PubMed ID: 8031538
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rare interstitial deletion (2)(p11.2p13) in a child with pericentric inversion (2)(p11.2q13) of paternal origin.
    Lacbawan FL; White BJ; Anguiano A; Rigdon DT; Ball KD; Bromage GB; Yang X; DiFazio MP; Levin SW
    Am J Med Genet; 1999 Nov; 87(2):139-42. PubMed ID: 10533028
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Interstitial deletion of the short arm of chromosome 1 (46XY, del(1)(p13p22.3)).
    Mattia FR; Wardinsky TD; Tuttle DJ; Grix A; Smith KA; Walling P
    Am J Med Genet; 1992 Nov; 44(5):551-4. PubMed ID: 1481806
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.