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 *

133 related articles for article (PubMed ID: 643350)

  • 1. Radiological abnormalities associated with anomalies of the ninth chromosome.
    Pilling DW; Levick RK
    Pediatr Radiol; 1978 Feb; 6(4):215-21. PubMed ID: 643350
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Nail-patella syndrome].
    Wildfeuer T; Albrecht G
    Hautarzt; 1996 Nov; 47(11):860-2. PubMed ID: 9036142
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Skeletal anomalies in nail-patella syndrome. Case report and overview].
    Höger PH; Henschel MG
    Hautarzt; 1997 Aug; 48(8):581-5. PubMed ID: 9378640
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The radiological pattern associated with the trisomy of the short arm of chromosome No 4.
    Dallapiccola B; Giovannelli G; Forabosco A
    Pediatr Radiol; 1975 Jan; 3(1):34-40. PubMed ID: 1233411
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Trisomy for the short arm of chromosome No. 10.
    Hustinx TW; Ter Haar BG; Scheres JM; Rutten FJ
    Clin Genet; 1974; 6(5):408-15. PubMed ID: 4434655
    [No Abstract]   [Full Text] [Related]  

  • 6. Partial trisomy 10q in three unrelated patients.
    Taysi K; Yang V; Monaghan N; Beraha N
    Ann Genet; 1983; 26(2):79-85. PubMed ID: 6604490
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Autosomal linkage in man: the nail-patella syndrome.
    Duthie RB
    Clin Orthop Relat Res; 1964; 33():129-37. PubMed ID: 5889017
    [No Abstract]   [Full Text] [Related]  

  • 8. Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9.
    Butler LJ; Eades SM; France NE
    Ann Genet; 1969 Mar; 12(1):15-27. PubMed ID: 5306708
    [No Abstract]   [Full Text] [Related]  

  • 9. Partial trisomy 12q: a clinically recognisable syndrome. Genetic risks associated with translocations of chromosome 12q.
    Pratt NR; Bulugahapitiya DT
    J Med Genet; 1983 Apr; 20(2):86-9. PubMed ID: 6842562
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial partial trisomy of the long arm of chromosome 10 (q24-26).
    Moreno-Fuenmayor H; Zackai EH; Mellman WJ; Aronson M
    Pediatrics; 1975 Nov; 56(5):756-61. PubMed ID: 1196732
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Radiological findings in two sisters with trisomy of the short arm of chromosome 4.
    Giovannelli G; Rossi L; Forabosco A
    Helv Paediatr Acta; 1973 Dec; 28(6):543-52. PubMed ID: 4785152
    [No Abstract]   [Full Text] [Related]  

  • 12. Partial trisomy 12q.
    Zabel B; Baumann W
    J Med Genet; 1981 Apr; 18(2):144-6. PubMed ID: 7241532
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8.
    Pai GS; Thomas GH; Leonard CO; Ward JC; Valle DL; Pyeritz RE
    Johns Hopkins Med J; 1979 Oct; 145(4):162-9. PubMed ID: 491337
    [No Abstract]   [Full Text] [Related]  

  • 14. Two chromosomal syndromes in the same family: monosomy and trisomy for part of the short arm of chromosome 10.
    Slinde S; Hansteen IL
    Eur J Pediatr; 1982 Oct; 139(2):153-7. PubMed ID: 7151837
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Influence of the parental Rhesus types on the segregation of genetic abnormalities.
    Nijenhuis LE
    Vox Sang; 1970; 19(5):496-507. PubMed ID: 4993883
    [No Abstract]   [Full Text] [Related]  

  • 16. A new syndrome resulting from partial trisomy for the distal third of the long arm of chromosome 10.
    Yunis JJ; Sanchez O
    J Pediatr; 1974 Apr; 84(4):567-70. PubMed ID: 4834252
    [No Abstract]   [Full Text] [Related]  

  • 17. Trisomy for the distal half of the short arm of chromosome 9. A variant of the trisomy 9p syndrome.
    Lewandowski RC; Yunis JJ; Lehrke R; O'Leary J; Swaiman KF; Sanchez O
    Am J Dis Child; 1976 Jun; 130(6):663-7. PubMed ID: 937286
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Prenatal diagnosis of a de novo trisomy case 9q-47,XX,+9 del(q33----qter)].
    Cordier MP; Coicaud C; Thoulon JM; Robert JM; Germain D
    J Genet Hum; 1984 Dec; 32(5):351-61. PubMed ID: 6527131
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary onycho-osteodysplasia (Nail-Patella syndrome). A report of nine kindreds.
    Beals RK; Eckhardt AL
    J Bone Joint Surg Am; 1969 Apr; 51(3):505-16. PubMed ID: 5778286
    [No Abstract]   [Full Text] [Related]  

  • 20. A familial 10/13 translocation: partial trisomy C in an infant associated with familial 10/13 translocation.
    Mulcahy MT; Jenkyn J; Masters PL
    Clin Genet; 1974; 6(5):335-40. PubMed ID: 4434650
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.