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 *

160 related articles for article (PubMed ID: 1538725)

  • 21. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.
    Knoll JH; Nicholls RD; Magenis RE; Graham JM; Lalande M; Latt SA
    Am J Med Genet; 1989 Feb; 32(2):285-90. PubMed ID: 2564739
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review.
    Nicholls RD
    Am J Med Genet; 1993 Apr; 46(1):16-25. PubMed ID: 8388169
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prader-Willi syndrome in siblings, due to unbalanced translocation between chromosomes 15 and 22.
    Fernandez F; Berry C; Mutton D
    Arch Dis Child; 1987 Aug; 62(8):841-3. PubMed ID: 3662590
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Characterization of a DNA sequence family in the Prader-Willi/Angelman syndrome chromosome region in 15q11-q13.
    Dittrich B; Knoblauch H; Buiting K; Horsthemke B
    Genomics; 1993 Apr; 16(1):269-71. PubMed ID: 8486372
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Genomic imprinting in an Angelman and Prader-Willi translocation family.
    Hultén M; Armstrong S; Challinor P; Gould C; Hardy G; Leedham P; Lee T; McKeown C
    Lancet; 1991 Sep; 338(8767):638-9. PubMed ID: 1679180
    [No Abstract]   [Full Text] [Related]  

  • 27. Angelman syndrome and prenatally diagnosed Prader-Willi syndrome in first cousins.
    Ranganath P; Agarwal M; Phadke SR
    Am J Med Genet A; 2011 Nov; 155A(11):2788-90. PubMed ID: 21964995
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Interstitial 15q deletion without a classic Prader-Willi phenotype.
    Galán F; Aguilar MS; González J; Clemente F; Sánchez R; Tapia M; Moya M
    Am J Med Genet; 1991 Mar; 38(4):532-4. PubMed ID: 2063892
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation.
    Calounova G; Novotna D; Simandlova M; Havlovicova M; Zumrová A; Kocarek E; Sedlacek Z
    Neuro Endocrinol Lett; 2006 Oct; 27(5):579-85. PubMed ID: 17159828
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Unbalanced translocation t (5;15) in a patient with Prader-Willi syndrome].
    Bai JL; Wang H; Yang YL; Song F
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Dec; 27(6):664-7. PubMed ID: 21154328
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetic basis of Prader-Willi syndrome in Korea: less uniparental disomy than has been recognized?
    Kim HJ; Cho HJ; Jin DK; Kwon EK; Ki CS; Kim JW; Kim SH
    Clin Genet; 2004 Oct; 66(4):368-72. PubMed ID: 15355442
    [No Abstract]   [Full Text] [Related]  

  • 32. Membranoproliferative glomerulonephritis in a child with Prader-Willi syndrome.
    Robson WL; Leung AK
    Am J Med Genet; 1992 Jul; 43(5):858-9. PubMed ID: 1642276
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The Prader-Willi syndrome with a 15/3 translocation.
    Kucerová M; Straková M; Polívková Z
    J Med Genet; 1979 Jun; 16(3):234-5. PubMed ID: 469905
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Unbalanced translocation (15;17)(q13;13.3) with apparent Prader-Willi syndrome but without Miller-Dieker syndrome.
    Elder FF; Nichols MM; Hood OJ; Harrison WR
    Am J Med Genet; 1985 Mar; 20(3):519-24. PubMed ID: 3993677
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The human genome: detecting chromosomal deletions: Angelman and Prader-Willi syndromes.
    Morris-Rosendahl DJ; Back E
    Am J Psychiatry; 2002 Mar; 159(3):372. PubMed ID: 11869997
    [No Abstract]   [Full Text] [Related]  

  • 36. 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]  

  • 37. Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint.
    Schulze A; Hansen C; Skakkebaek NE; Brøndum-Nielsen K; Ledbeter DH; Tommerup N
    Nat Genet; 1996 Apr; 12(4):452-4. PubMed ID: 8630505
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. [Prader-Willi syndrome and translocation 15/15].
    Tylki A; Lech H; Gurkau M; Parcheta B
    Ann Genet; 1982; 25(3):183-4. PubMed ID: 6982673
    [No Abstract]   [Full Text] [Related]  

  • 40. [Cytogenetic detection of Prader-Willi syndrome in infancy].
    Götz J; Krüger G; Westphal BC; Pelz L
    Kinderarztl Prax; 1989 May; 57(5):239-43. PubMed ID: 2747122
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.