BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 3688018)

  • 1. 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]  

  • 2. The cytogenetic controversy in the Prader-Labhart-Willi syndrome.
    Kousseff BG
    Am J Med Genet; 1982 Dec; 13(4):431-9. PubMed ID: 7158643
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 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. [Chromosome aberrations in Prader-Willi-Labhart syndrome--critical review, documented by 4 unusual cases].
    Pfeiffer RA; Tschech L; Irle U; Wündisch GF
    Klin Padiatr; 1987; 199(5):329-35. PubMed ID: 3316824
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter-->Xq26.1::15p11-->15qter).
    Scheuerle A; Zenger-Hain JL; Van Dyke DL; Ledbetter DH; Greenberg F; Shaffer LG
    Am J Med Genet; 1995 May; 56(4):403-8. PubMed ID: 7604850
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [Prader-Labhart-Willi syndrome in infants].
    Schmeling H; Gillessen-Kaesbach G; Schulte-Mattler U; Burdach S; Horneff G
    Klin Padiatr; 2002; 214(2):51-3. PubMed ID: 11972309
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Kleine-Levin syndrome in a boy with Prader-Willi syndrome.
    Gau SF; Soong WT; Liu HM; Hou JW; Tsai WY; Chiu YN; Yeh YC; Wang PJ; Wang TR
    Sleep; 1996 Jan; 19(1):13-7. PubMed ID: 8650457
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons.
    Williams CA; Gray BA; Hendrickson JE; Stone JW; Cantú ES
    Am J Med Genet; 1989 Mar; 32(3):339-45. PubMed ID: 2786338
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mosaic paternally derived inv dup(15) may partially rescue the Prader-Willi syndrome phenotype with uniparental disomy.
    Saitoh S; Hosoki K; Takano K; Tonoki H
    Clin Genet; 2007 Oct; 72(4):378-80. PubMed ID: 17850637
    [No Abstract]   [Full Text] [Related]  

  • 15. Sister chromatid exchange analysis in the Prader-Labhart-Willi syndrome.
    Butler MG; Jenkins BB
    Am J Med Genet; 1987 Dec; 28(4):821-7. PubMed ID: 3688020
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Is Angelman syndrome an alternate result of del(15)(q11q13)?
    Magenis RE; Brown MG; Lacy DA; Budden S; LaFranchi S
    Am J Med Genet; 1987 Dec; 28(4):829-38. PubMed ID: 3688021
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inv dup(15) supernumerary marker chromosomes.
    Webb T
    J Med Genet; 1994 Aug; 31(8):585-94. PubMed ID: 7815414
    [No Abstract]   [Full Text] [Related]  

  • 18. [Self-induced cutaneous lesions in Prader-Willi syndrome].
    Plantin P; Milochau P; Broussine L; Blondin G
    Ann Dermatol Venereol; 1997; 124(5):390-2. PubMed ID: 9739896
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of chromosome breakage in the Prader-Labhart-Willi syndrome.
    Butler MG; Jenkins BB
    Am J Med Genet; 1989 Apr; 32(4):514-9. PubMed ID: 2505618
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Y/15 translocation in a 45,X male with Prader-Willi syndrome.
    Puvabanditsin S; Garrow E; Razi S; Mohar AG; Tadros JJ; Phattraprayoon N; Patel P
    Genet Couns; 2007; 18(4):417-21. PubMed ID: 18286823
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.