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 *

370 related articles for article (PubMed ID: 1632436)

  • 1. Unique karyotypes in two patients with Prader-Willi syndrome.
    Narahara K; Hiramoto K; Murakami M; Miyake S; Tsuji K; Yokoyama Y; Namba H; Ninomiya S; Murakami R; Seino Y
    Am J Med Genet; 1992 Mar; 42(5):671-7. PubMed ID: 1632436
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population.
    Cassidy SB; Thuline HC; Holm VA
    Am J Med Genet; 1984 Feb; 17(2):485-95. PubMed ID: 6336316
    [TBL] [Abstract][Full Text] [Related]  

  • 3. True telomeric translocation in a baby with the Prader-Willi phenotype.
    Reeve A; Norman A; Sinclair P; Whittington-Smith R; Hamey Y; Donnai D; Read A
    Am J Med Genet; 1993 Aug; 47(1):1-6. PubMed ID: 8368237
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Duplication of proximal 15q as a cause of Prader-Willi syndrome.
    Pettigrew AL; Gollin SM; Greenberg F; Riccardi VM; Ledbetter DH
    Am J Med Genet; 1987 Dec; 28(4):791-802. PubMed ID: 3688017
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical comparison of 59 Prader-Willi patients with and without the 15(q12) deletion.
    Wenger SL; Hanchett JM; Steele MW; Maier BV; Golden WL
    Am J Med Genet; 1987 Dec; 28(4):881-7. PubMed ID: 3688026
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Deletions of proximal 15q without Prader-Willi syndrome.
    Greenberg F; Ledbetter DH
    Am J Med Genet; 1987 Dec; 28(4):813-20. PubMed ID: 3688019
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Atypical phenotype associated with deletion (15) (pter----q11::q13----qter).
    Reynolds JF; Daniel A; FitzGerald J
    Am J Med Genet; 1987 Sep; 28(1):55-8. PubMed ID: 3674118
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Neonatal diagnosis of Prader-Willi syndrome and its implications.
    Greenberg F; Elder FF; Ledbetter DH
    Am J Med Genet; 1987 Dec; 28(4):845-56. PubMed ID: 3688023
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR.
    Gregory CA; Kirkilionis AJ; Greenberg CR; Chudley AE; Hamerton JL
    Am J Med Genet; 1990 Apr; 35(4):536-45. PubMed ID: 1970703
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish.
    Engelen JJ; Loots WJ; Albrechts JC; Schrander-Stumpel CT; Dirckx R; Smeets HJ; Hamers AJ; Geraedts JP
    Genet Couns; 1999; 10(2):123-32. PubMed ID: 10422004
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular and clinical overlap of Angelman and Prader-Willi syndrome phenotypes.
    Kirkilionis AJ; Chudley AE; Gregory CA; Hamerton JL
    Am J Med Genet; 1991 Sep; 40(4):454-9. PubMed ID: 1684091
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular markers for diagnosis of Prader-Willi syndrome in thai patients by fish.
    Wiriyaukaradecha S; Patmasiriwat P; Wasant P; Tantiniti P
    Southeast Asian J Trop Med Public Health; 2003 Dec; 34(4):881-6. PubMed ID: 15115105
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Unique mosaicism in Prader-Labhart-Willi syndrome--a contiguous gene or aneuploidy syndrome?
    Kousseff BG; Diamond T; Essig Y; Miller K; Tedesco T
    Am J Med Genet; 1987 Dec; 28(4):803-11. PubMed ID: 3688018
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deletion of chromosome 15pter-->q11.2 due to t(Y;15) in a boy with Prader-Willi syndrome.
    Qumsiyeh MB; Dalton JD; Gordon PL; Wilroy RS; Tharapel AT
    Am J Med Genet; 1992 Jan; 42(1):109-11. PubMed ID: 1308348
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences.
    Magenis RE; Toth-Fejel S; Allen LJ; Black M; Brown MG; Budden S; Cohen R; Friedman JM; Kalousek D; Zonana J
    Am J Med Genet; 1990 Mar; 35(3):333-49. PubMed ID: 2309780
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and cytogenetic studies of the Prader-Willi syndrome: evidence of phenotype-karyotype correlation.
    Niikawa N; Ishikiriyama S
    Hum Genet; 1985; 69(1):22-7. PubMed ID: 3855404
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases.
    Ledbetter DH; Mascarello JT; Riccardi VM; Harper VD; Airhart SD; Strobel RJ
    Am J Hum Genet; 1982 Mar; 34(2):278-85. PubMed ID: 7072717
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15).
    Varela MC; Lopes GM; Koiffmann CP
    Ann Genet; 2004; 47(3):267-73. PubMed ID: 15337472
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A case of Prader Willi syndrome with del 15 (q11-->q13).
    Tunçman G; Tükün A; Yalaz K; Bökesoy I
    Turk J Pediatr; 1993; 35(4):333-6. PubMed ID: 8160287
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Non-reciprocal translocation (5;15), isodicentric (15) and Prader-Willi syndrome.
    Murdock RL; Wurster-Hill DH
    Am J Med Genet; 1986 Sep; 25(1):61-9. PubMed ID: 3799724
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.