BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

190 related articles for article (PubMed ID: 1679180)

  • 1. 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]  

  • 2. 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]  

  • 3. Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences.
    Buiting K; Neumann M; Lüdecke HJ; Senger G; Claussen U; Antich J; Passarge E; Horsthemke B
    Genomics; 1990 Mar; 6(3):521-7. PubMed ID: 2328991
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Prader-Willi and Angelman syndromes: update on genetic mechanisms and diagnostic complexities.
    Khan NL; Wood NW
    Curr Opin Neurol; 1999 Apr; 12(2):149-54. PubMed ID: 10226746
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15.
    Smeets DF; Hamel BC; Nelen MR; Smeets HJ; Bollen JH; Smits AP; Ropers HH; van Oost BA
    N Engl J Med; 1992 Mar; 326(12):807-11. PubMed ID: 1538725
    [No Abstract]   [Full Text] [Related]  

  • 7. Prader-Willi and Angelman syndromes. Disorders of genomic imprinting.
    Cassidy SB; Schwartz S
    Medicine (Baltimore); 1998 Mar; 77(2):140-51. PubMed ID: 9556704
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Prader-Willi syndrome and Robertsonian translocations involving chromosome 15.
    Casamassima AC; Shapiro LR; Wilmot PL; Smith KB
    Clin Genet; 1991 Apr; 39(4):294-7. PubMed ID: 1817468
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Atypical Prader-Willi and 15q13.3 Microdeletion Syndromes in a Patient with an Unbalanced Translocation.
    Colovati MES; Grossi BM; Nunes GD; Fock RA; Guedes DR; Melaragno MI; Cernach MCSP
    Cytogenet Genome Res; 2019; 158(4):192-198. PubMed ID: 31394532
    [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. Microdeletion 15q26.2qter and Microduplication 18q23 in a Patient with Prader-Willi-Like Syndrome: Clinical Findings.
    Dello Russo P; Demori E; Sechi A; Passon N; Romagno D; Gnan C; Zoratti R; Damante G
    Cytogenet Genome Res; 2016; 148(1):14-8. PubMed ID: 27160288
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chromosome 15 in Prader-Willi syndrome.
    Fear CN; Mutton DE; Berry AC; Heckmatt JZ; Dubowitz V
    Dev Med Child Neurol; 1985 Jun; 27(3):305-11. PubMed ID: 4018424
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
    Clayton-Smith J; Driscoll DJ; Waters MF; Webb T; Andrews T; Malcolm S; Pembrey ME; Nicholls RD
    Am J Med Genet; 1993 Oct; 47(5):683-6. PubMed ID: 8266996
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 'Severe' Prader-Willi syndrome with a large deletion of chromosome 15 due to an unbalanced t(15,22)(q14;q11.2) translocation.
    Matsumura M; Kubota T; Hidaka E; Wakui K; Kadowaki S; Ueta I; Shimizu T; Ueno I; Yamauchi K; Herzing LB; Nurmi EL; Sutcliffe JS; Fukushima Y; Katsuyama T
    Clin Genet; 2003 Jan; 63(1):79-81. PubMed ID: 12519378
    [No Abstract]   [Full Text] [Related]  

  • 17. Form of 15q proximal duplication appears to be a normal euchromatic variant.
    Jalal SM; Persons DL; Dewald GW; Lindor NM
    Am J Med Genet; 1994 Oct; 52(4):495-7. PubMed ID: 7747767
    [No Abstract]   [Full Text] [Related]  

  • 18. Genomic imprinting and human chromosome 15.
    Repetto GM
    Biol Res; 2001; 34(2):141-5. PubMed ID: 11715207
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.
    Kalsner L; Chamberlain SJ
    Pediatr Clin North Am; 2015 Jun; 62(3):587-606. PubMed ID: 26022164
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.