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 *

87 related articles for article (PubMed ID: 308342)

  • 41. Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation.
    Serra A; Bova R; Bellanova G; Chindemi A; Zappata S; Brahe C
    Am J Med Genet; 1997 Aug; 71(2):139-43. PubMed ID: 9217211
    [TBL] [Abstract][Full Text] [Related]  

  • 42. A clinical syndrome associated with 5p duplication and 9p deletion.
    Liberfarb RM; Atkins L; Holmes LB
    Ann Genet; 1980; 23(1):26-30. PubMed ID: 6965836
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Choanal atresia in a patient with the deletion (9p) syndrome.
    Shashi V; Golden WL; Fryburg JS
    Am J Med Genet; 1994 Jan; 49(1):88-90. PubMed ID: 8172257
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 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]  

  • 45. The distal 9p trisomy syndrome: a major clinical-cytogenetic entity.
    Centerwall WR
    Birth Defects Orig Artic Ser; 1977; 13(3D):165-77. PubMed ID: 922135
    [No Abstract]   [Full Text] [Related]  

  • 46. Langer-Giedion syndrome with interstitial 8q-deletion.
    Zabel BU; Baumann WA
    Am J Med Genet; 1982 Mar; 11(3):353-8. PubMed ID: 7081298
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 4p trisomy syndrome: report of 4 additional cases and segregation analysis of 21 families with different translocations.
    Crane J; Sujansky E; Smith A
    Am J Med Genet; 1979; 4(3):219-29. PubMed ID: 517577
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [A case of partial 9p monosomy].
    Monteverde R; Gimelli G; Cuoco C; Porta S; Lattere M
    Minerva Pediatr; 1983 Nov; 35(22):1133-6. PubMed ID: 6672601
    [No Abstract]   [Full Text] [Related]  

  • 49. Long arm deletion of chromosome no. 6 in a mentally retarded boy with multiple physical malformations.
    Milosević J; Kalicanin P
    J Ment Defic Res; 1975 Jun; 19(2):139-44. PubMed ID: 1195357
    [TBL] [Abstract][Full Text] [Related]  

  • 50. A specific syndrome due to deletion of the distal long arm of chromosome 1.
    Meinecke P; Vögtel D
    Am J Med Genet; 1987 Oct; 28(2):371-6. PubMed ID: 3322005
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Phenotypic and cytogenetic analysis of an unusual malformative syndrome (trisomy 9 p+)].
    Chipail A; Constantinescu V; Covic M; Angheloni T
    Rev Pediatr Obstet Ginecol Pediatr; 1976; 25(3):201-10. PubMed ID: 11544
    [No Abstract]   [Full Text] [Related]  

  • 52. Possible intrachromosomal duplication in a case of trisomy 9p.
    Chiyo H; Furuyama J; Suehara N; Obashi Y; Kikkawa H
    Hum Genet; 1976 Oct; 34(2):217-21. PubMed ID: 1002145
    [TBL] [Abstract][Full Text] [Related]  

  • 53. De novo trisomy 9pter leads to q13.
    Kardon NB; Salwen HR; Krauss MA; Davis JG; Jenkins EC
    Hum Genet; 1977 Jun; 37(2):149-53. PubMed ID: 885535
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Trisomy 9p. Report of two new cases].
    San Román Muñoz M; Herranz Fernández JL; Tejerina Puente A; Arteaga Manjón-Cabeza R; López Grondona F
    An Pediatr (Barc); 2004 Oct; 61(4):336-9. PubMed ID: 15456590
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 9p Trisomy/18p distal monosomy and multiple cutaneous leiomyomata. Another specific chromosomal site (18pter) in dominantly inherited multiple tumors?
    Fryns JP; Haspeslagh M; de Mûelenaere A; van Den Berghe H
    Hum Genet; 1985; 70(3):284-6. PubMed ID: 4018793
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Duplication of the short arm of chromosome 9. Analysis of five cases.
    Cuoco C; Gimelli G; Pasquali F; Poloni L; Zuffardi O; Alicata P; Battaglino G; Bernardi F; Cerone R; Cotellessa M; Ghidoni A; Motta S
    Hum Genet; 1982; 61(1):3-7. PubMed ID: 7129421
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Trisomy 9 (pter----q1 to q3): the phenotype as an objective aid to karyotypic interpretation.
    Preus M; Schinzel A; Aymé S; Kaijser K
    Clin Genet; 1984 Jul; 26(1):52-5. PubMed ID: 6467656
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Eleven new cases of del(9p) and features from 80 cases.
    Huret JL; Leonard C; Forestier B; Rethoré MO; Lejeune J
    J Med Genet; 1988 Nov; 25(11):741-9. PubMed ID: 3070043
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Two new cases of 9p- syndrome.
    Wiśniewski L; Szymańska J; Niezabitowska A; Krajewska-Walasek M; Mospinek-Krasnopolska M
    Klin Padiatr; 1980 May; 192(3):270-4. PubMed ID: 7191928
    [TBL] [Abstract][Full Text] [Related]  

  • 60. 9p trisomy identified by Giemsa-11.
    Wyandt HE; Hecht F; Magenis RE; Wysham DG; Prescott G
    Hum Genet; 1976 Mar; 31(3):355-8. PubMed ID: 955631
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.