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 *

194 related articles for article (PubMed ID: 9279757)

  • 1. Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome families.
    Gilbert HL; Buxton JL; Chan CT; McKay T; Cottrell S; Ramsden S; Winter RM; Pembrey ME; Malcolm S
    J Med Genet; 1997 Aug; 34(8):651-5. PubMed ID: 9279757
    [TBL] [Abstract][Full Text] [Related]  

  • 2. DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprinting.
    Glenn CC; Deng G; Michaelis RC; Tarleton J; Phelan MC; Surh L; Yang TP; Driscoll DJ
    Prenat Diagn; 2000 Apr; 20(4):300-6. PubMed ID: 10740202
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.
    Saitoh S; Buiting K; Cassidy SB; Conroy JM; Driscoll DJ; Gabriel JM; Gillessen-Kaesbach G; Glenn CC; Greenswag LR; Horsthemke B; Kondo I; Kuwajima K; Niikawa N; Rogan PK; Schwartz S; Seip J; Williams CA; Nicholls RD
    Am J Med Genet; 1997 Jan; 68(2):195-206. PubMed ID: 9028458
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients.
    Glenn CC; Nicholls RD; Robinson WP; Saitoh S; Niikawa N; Schinzel A; Horsthemke B; Driscoll DJ
    Hum Mol Genet; 1993 Sep; 2(9):1377-82. PubMed ID: 8242060
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.
    Reis A; Dittrich B; Greger V; Buiting K; Lalande M; Gillessen-Kaesbach G; Anvret M; Horsthemke B
    Am J Hum Genet; 1994 May; 54(5):741-7. PubMed ID: 8178815
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.
    Buiting K; Saitoh S; Gross S; Dittrich B; Schwartz S; Nicholls RD; Horsthemke B
    Nat Genet; 1995 Apr; 9(4):395-400. PubMed ID: 7795645
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome.
    Horsthemke B; Maat-Kievit A; Sleegers E; van den Ouweland A; Buiting K; Lich C; Mollevanger P; Beverstock G; Gillessen-Kaesbach G; Schwanitz G
    J Med Genet; 1996 Oct; 33(10):848-51. PubMed ID: 8933339
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15.
    Runte M; Färber C; Lich C; Zeschnigk M; Buchholz T; Smith A; Van Maldergem L; Bürger J; Muscatelli F; Gillessen-Kaesbach G; Horsthemke B; Buiting K
    Eur J Hum Genet; 2001 Jul; 9(7):519-26. PubMed ID: 11464243
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Cloning of the breakpoints of a submicroscopic deletion in an Angelman syndrome patient.
    Greger V; Woolf E; Lalande M
    Hum Mol Genet; 1993 Jul; 2(7):921-4. PubMed ID: 8364575
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region.
    Knoll JH; Cheng SD; Lalande M
    Nat Genet; 1994 Jan; 6(1):41-6. PubMed ID: 8136833
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect.
    De Molfetta GA; Felix TM; Riegel M; Ferraz VE; de Pina Neto JM
    Arq Neuropsiquiatr; 2002 Dec; 60(4):1011-4. PubMed ID: 12563398
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
    Depienne C; Moreno-De-Luca D; Heron D; Bouteiller D; Gennetier A; Delorme R; Chaste P; Siffroi JP; Chantot-Bastaraud S; Benyahia B; Trouillard O; Nygren G; Kopp S; Johansson M; Rastam M; Burglen L; Leguern E; Verloes A; Leboyer M; Brice A; Gillberg C; Betancur C
    Biol Psychiatry; 2009 Aug; 66(4):349-59. PubMed ID: 19278672
    [TBL] [Abstract][Full Text] [Related]  

  • 15. FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromes.
    Teshima I; Chadwick D; Chitayat D; Kobayashi J; Ray P; Shuman C; Siegel-Bartelt J; Strasberg P; Weksberg R
    Am J Med Genet; 1996 Mar; 62(3):217-23. PubMed ID: 8882776
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.
    Saitoh S; Buiting K; Rogan PK; Buxton JL; Driscoll DJ; Arnemann J; König R; Malcolm S; Horsthemke B; Nicholls RD
    Proc Natl Acad Sci U S A; 1996 Jul; 93(15):7811-5. PubMed ID: 8755558
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial interstitial 570 kbp deletion of the UBE3A gene region causing Angelman syndrome but not Prader-Willi syndrome.
    Bürger J; Horn D; Tönnies H; Neitzel H; Reis A
    Am J Med Genet; 2002 Aug; 111(3):233-7. PubMed ID: 12210318
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Somatic and germ-line mosaicism of deletion 15q11.2-q13 in a mother of dyzigotic twins with Angelman syndrome.
    Sánchez J; Fernández R; Madruga M; Bernabeu-Wittel J; Antiñolo G; Borrego S
    Am J Med Genet A; 2014 Feb; 164A(2):370-6. PubMed ID: 24311297
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The mechanisms involved in formation of deletions and duplications of 15q11-q13.
    Robinson WP; Dutly F; Nicholls RD; Bernasconi F; Peñaherrera M; Michaelis RC; Abeliovich D; Schinzel AA
    J Med Genet; 1998 Feb; 35(2):130-6. PubMed ID: 9580159
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.