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 *

140 related articles for article (PubMed ID: 10213052)

  • 1. Two cases of maternal uniparental disomy 14 with a phenotype overlapping with the Prader-Willi phenotype.
    Berends MJ; Hordijk R; Scheffer H; Oosterwijk JC; Halley DJ; Sorgedrager N
    Am J Med Genet; 1999 May; 84(1):76-9. PubMed ID: 10213052
    [No Abstract]   [Full Text] [Related]  

  • 2. [Maternal uniparental disomy 14; differential diagnosis with Prader-Willi syndrome].
    Tamminga S; Stalman SE; Kamp GA; Hendriks YM; Knegt AC; Elting MW
    Ned Tijdschr Geneeskd; 2015; 159():A8240. PubMed ID: 25898865
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with mosaic trisomy 15.
    Olander E; Stamberg J; Steinberg L; Wulfsberg EA
    Am J Med Genet; 2000 Jul; 93(3):215-8. PubMed ID: 10925385
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Maternal uniparental disomy 14 syndrome demonstrates prader-willi syndrome-like phenotype.
    Hosoki K; Kagami M; Tanaka T; Kubota M; Kurosawa K; Kato M; Uetake K; Tohyama J; Ogata T; Saitoh S
    J Pediatr; 2009 Dec; 155(6):900-903.e1. PubMed ID: 19800077
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Temple syndrome as a differential diagnosis to Prader-Willi syndrome: Identifying three new patients.
    Lande A; Kroken M; Rabben K; Retterstøl L
    Am J Med Genet A; 2018 Jan; 176(1):175-180. PubMed ID: 29159982
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Case of 15q26-qter deletion associated with a Prader-Willi phenotype.
    Santos JFD; Acosta AX; Scheibler GG; Pitanga PML; Alves ES; Meira JGC; Zanardo ÉA; Kulikowski LD; Lima RLLF; Carvalho AFL
    Eur J Med Genet; 2020 Aug; 63(8):103955. PubMed ID: 32473228
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Exclusion of maternal uniparental disomy of chromosome 14 in patients referred for Prader-Willi syndrome using a multiplex methylation polymerase chain reaction assay.
    Dietz LG; Wylie AA; Rauen KA; Murphy SK; Jirtle RL; Cotter PD
    J Med Genet; 2003 Apr; 40(4):e46. PubMed ID: 12676919
    [No Abstract]   [Full Text] [Related]  

  • 8. Maternal UPD(14) in the patient with a normal karyotype: clinical report and a systematic search for cases in samples sent for testing for Prader-Willi syndrome.
    Cox H; Bullman H; Temple IK
    Am J Med Genet A; 2004 May; 127A(1):21-25. PubMed ID: 15103712
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Maternal uniparental disomy 14 in a 15-year-old boy with normal karyotype and no evidence of precocious puberty.
    Aretz S; Raff R; Woelfle J; Zerres K; Esser M; Propping P; Eggermann T
    Am J Med Genet A; 2005 Jun; 135(3):336-8. PubMed ID: 15887281
    [No Abstract]   [Full Text] [Related]  

  • 10. Paternal uniparental isodisomy for chromosome 14 in a patient with a normal 46,XY karyotype.
    Chu C; Schwartz S; McPherson E
    Am J Med Genet A; 2004 Jun; 127A(2):167-71. PubMed ID: 15108205
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Difficulties of genetic counseling and prenatal diagnosis in a consanguineous couple segregating for the same translocation (14;15) (q11;q13) and at risk for Prader-Willi and Angelman syndromes.
    Flori E; Biancalana V; Girard-Lemaire F; Favre R; Flori J; Doray B; Mandel JL
    Eur J Hum Genet; 2004 Mar; 12(3):181-6. PubMed ID: 14694357
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Maternal uniparental disomy 15 in a fetus resulting from a balanced familial translocation t(2;15)(p11;q11.2).
    Heidemann S; Plendl H; Vater I; Gesk S; Exeler-Telker JR; Grote W; Siebert R; Caliebe A
    Prenat Diagn; 2010 Feb; 30(2):183-5. PubMed ID: 20063327
    [No Abstract]   [Full Text] [Related]  

  • 14. Duplication or insertion in 15q11-13 associated with mental retardation-short stature and obesity-Prader-Willi or Cohen syndrome?
    Fuhrmann-Rieger A; Köhler A; Fuhrmann W
    Clin Genet; 1984 Apr; 25(4):347-52. PubMed ID: 6713711
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 in a boy with a balanced 3;21 translocation.
    Bassett LL; Michaelis RC; Geiger MH; Tarleton J; Moore CL; Knops JF; Carroll AJ; Proud VK
    Am J Med Genet; 2001 Apr; 100(1):85-6. PubMed ID: 11337756
    [No Abstract]   [Full Text] [Related]  

  • 16. [Spread of X-chromosome inactivation into chromosome 15 is associated with Prader Willi syndrome phenotype in a boy with a t (X ; 15) (p21.1 ; q11.2) translocation].
    Sakazume S
    No To Hattatsu; 2014 Mar; 46(2):121-4. PubMed ID: 24738189
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. Maladaptive behavior differences in Prader-Willi syndrome due to paternal deletion versus maternal uniparental disomy.
    Dykens EM; Cassidy SB; King BH
    Am J Ment Retard; 1999 Jan; 104(1):67-77. PubMed ID: 9972835
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular cytogenetics of Prader-Willi and Angelman syndromes.
    Hultén M; Hardy G; Gould C; Stergianou R; Waters J; McKeown C
    Lancet; 1992 Jan; 339(8787):243-4. PubMed ID: 1346195
    [No Abstract]   [Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 7.