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 *

291 related articles for article (PubMed ID: 27570435)

  • 1. Prader-Willi Syndrome: Clinical and Genetic Findings.
    Butler MG; Thompson T
    Endocrinologist; 2000 Jul; 10(4 Suppl 1):3S-16S. PubMed ID: 27570435
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deletion analysis of the imprinting center region in patients with Angelman syndrome and Prader-Willi syndrome by real-time quantitative PCR.
    Raca G; Buiting K; Das S
    Genet Test; 2004; 8(4):387-94. PubMed ID: 15684868
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. 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]  

  • 5. Influence of the Prader-Willi syndrome imprinting center on the DNA methylation landscape in the mouse brain.
    Brant JO; Riva A; Resnick JL; Yang TP
    Epigenetics; 2014 Nov; 9(11):1540-56. PubMed ID: 25482058
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Baby food and bedtime: Evidence for opposite phenotypes from different genetic and epigenetic alterations in Prader-Willi and Angelman syndromes.
    Salminen II; Crespi BJ; Mokkonen M
    SAGE Open Med; 2019; 7():2050312118823585. PubMed ID: 30728968
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Diagnosis of Prader-Willi syndrome and Angelman syndrome by targeted nanopore long-read sequencing.
    Yamada M; Okuno H; Okamoto N; Suzuki H; Miya F; Takenouchi T; Kosaki K
    Eur J Med Genet; 2023 Feb; 66(2):104690. PubMed ID: 36587803
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evolution of genomic imprinting with biparental care: implications for Prader-Willi and Angelman syndromes.
    Ubeda F
    PLoS Biol; 2008 Aug; 6(8):e208. PubMed ID: 18752349
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Molecular diagnosis of Prader-Willi and Angelman syndromes: methylation, cytogenetics and FISH analysis].
    Santa María L; Curotto B; Cortés F; Rojas C; Alliende MA
    Rev Med Chil; 2001 Apr; 129(4):367-74. PubMed ID: 11413988
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology.
    Gold JA; Ruth C; Osann K; Flodman P; McManus B; Lee HS; Donkervoort S; Khare M; Roof E; Dykens E; Miller JL; Driscoll DJ; Butler MG; Heinemann J; Cassidy S; Kimonis VE
    Genet Med; 2014 Feb; 16(2):164-9. PubMed ID: 23928912
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [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]  

  • 13. Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E).
    Nakao M; Sutcliffe JS; Durtschi B; Mutirangura A; Ledbetter DH; Beaudet AL
    Hum Mol Genet; 1994 Feb; 3(2):309-15. PubMed ID: 8004100
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Transmission of a Novel Imprinting Center Deletion Associated With Prader-Willi Syndrome Through Three Generations of a Chinese Family: Case Presentation, Differential Diagnosis, and a Lesson Worth Thinking About.
    Zhang K; Liu S; Gu W; Lv Y; Yu H; Gao M; Wang D; Zhao J; Li X; Gai Z; Zhao S; Liu Y; Yuan Y
    Front Genet; 2021; 12():630650. PubMed ID: 34504512
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prader-Labhart-Willi syndrome.
    Anavi Y; Mintz SM
    Ann Dent; 1990; 49(2):26-9. PubMed ID: 2278477
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The Prader-Willi syndrome: a study of 40 patients and a review of the literature.
    Bray GA; Dahms WT; Swerdloff RS; Fiser RH; Atkinson RL; Carrel RE
    Medicine (Baltimore); 1983 Mar; 62(2):59-80. PubMed ID: 6338343
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Glucose homeostasis in Prader-Willi syndrome and potential implications of growth hormone therapy.
    Zipf WB
    Acta Paediatr Suppl; 1999 Dec; 88(433):115-7. PubMed ID: 10626560
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prader-Willi syndrome: clinical and molecular cytogenetic investigations.
    Hou JW; Wang TR
    J Formos Med Assoc; 1996 Jun; 95(6):474-9. PubMed ID: 8772055
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The genetic basis for Prader-Willi syndrome: the importance of imprinted genes.
    Brøndum-Nielsen K
    Acta Paediatr Suppl; 1997 Nov; 423():55-7. PubMed ID: 9401540
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Imprinted genes in the Prader-Willi deletion.
    Francke U
    Novartis Found Symp; 1998; 214():264-75; discussion 275-9. PubMed ID: 9601023
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.