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 *

142 related articles for article (PubMed ID: 17537021)

  • 1. Genotype and phenotype in patients with Prader-Willi syndrome in Taiwan.
    Lin HY; Lin SP; Chuang CK; Chen MR; Yen JL; Lee YJ; Huang CY; Tsai LP; Niu DM; Chao MC; Kuo PL
    Acta Paediatr; 2007 Jun; 96(6):902-5. PubMed ID: 17537021
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype-phenotype correlation in Prader-Willi syndrome: A large-sample analysis in China.
    Mao S; Yang L; Gao Y; Zou C
    Clin Genet; 2024 Apr; 105(4):415-422. PubMed ID: 38258470
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular subtype and growth hormone effects on dysmorphology in Prader-Willi syndrome.
    Oldzej J; Manazir J; Gold JA; Mahmoud R; Osann K; Flodman P; Cassidy SB; Kimonis VE
    Am J Med Genet A; 2020 Jan; 182(1):169-175. PubMed ID: 31782896
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Congenital ichthyosis in Prader-Willi syndrome associated with maternal chromosome 15 uniparental disomy: Case report and review of autosomal recessive conditions unmasked by UPD.
    Muthusamy K; Macke EL; Klee EW; Tebben PJ; Hand JL; Hasadsri L; Marcou CA; Schimmenti LA
    Am J Med Genet A; 2020 Oct; 182(10):2442-2449. PubMed ID: 32815268
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Relationship between phenotype and genotype of 102 Chinese newborns with Prader-Willi syndrome.
    Ge MM; Gao YY; Wu BB; Yan K; Qin Q; Wang H; Zhou W; Yang L
    Mol Biol Rep; 2019 Oct; 46(5):4717-4724. PubMed ID: 31270759
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic subtypes and phenotypic characteristics of 110 patients with Prader-Willi syndrome.
    Zhang L; Liu X; Zhao Y; Wang Q; Zhang Y; Gao H; Zhang B; Cui W; Zhao Y
    Ital J Pediatr; 2022 Jul; 48(1):121. PubMed ID: 35870983
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients.
    Varela MC; Kok F; Setian N; Kim CA; Koiffmann CP
    Clin Genet; 2005 Jan; 67(1):47-52. PubMed ID: 15617548
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria.
    Gunay-Aygun M; Schwartz S; Heeger S; O'Riordan MA; Cassidy SB
    Pediatrics; 2001 Nov; 108(5):E92. PubMed ID: 11694676
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comparison of perinatal factors in deletion versus uniparental disomy in Prader-Willi syndrome.
    Gold JA; Mahmoud R; Cassidy SB; Kimonis V
    Am J Med Genet A; 2018 May; 176(5):1161-1165. PubMed ID: 29681103
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. A girl with incomplete Prader-Willi syndrome and negative MS-PCR, found to have mosaic maternal UPD-15 at SNP array.
    Morandi A; Bonnefond A; Lobbens S; Carotenuto M; Del Giudice EM; Froguel P; Maffeis C
    Am J Med Genet A; 2015 Nov; 167A(11):2720-6. PubMed ID: 26109092
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prader-Willi syndrome in Taiwan.
    Lin HY; Lin SP; Yen JL; Lee YJ; Huang CY; Hung HY; Hsu CH; Kao HA; Chang JH; Chiu NC; Ho CS; Chao MC; Niu DM; Tsai LP; Kuo PL
    Pediatr Int; 2007 Jun; 49(3):375-9. PubMed ID: 17532839
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical-etiologic correlation in children with Prader-Willi syndrome (PWS): an interdisciplinary study.
    Torrado M; Araoz V; Baialardo E; Abraldes K; Mazza C; Krochik G; Ozuna B; Leske V; Caino S; Fano V; Chertkoff L
    Am J Med Genet A; 2007 Mar; 143A(5):460-8. PubMed ID: 17163531
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15.
    Cassidy SB; Forsythe M; Heeger S; Nicholls RD; Schork N; Benn P; Schwartz S
    Am J Med Genet; 1997 Feb; 68(4):433-40. PubMed ID: 9021017
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Why is there no diploid overdose effect in Prader-Willi syndrome due to uniparental disomy?
    Smith A
    Acta Genet Med Gemellol (Roma); 1996; 45(1-2):179-89. PubMed ID: 8872029
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prader-Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15--case report plus review of similar cases.
    Liehr T; Brude E; Gillessen-Kaesbach G; König R; Mrasek K; von Eggeling F; Starke H
    Eur J Med Genet; 2005; 48(2):175-81. PubMed ID: 16053909
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical Application of an Innovative Multiplex-Fluorescent-Labeled STRs Assay for Prader-Willi Syndrome and Angelman Syndrome.
    Zhang K; Liu S; Feng B; Yang Y; Zhang H; Dong R; Liu Y; Gai Z
    PLoS One; 2016; 11(2):e0147824. PubMed ID: 26841067
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD.
    Bittel DC; Kibiryeva N; Talebizadeh Z; Butler MG
    J Med Genet; 2003 Aug; 40(8):568-74. PubMed ID: 12920063
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype.
    Milner KM; Craig EE; Thompson RJ; Veltman MW; Thomas NS; Roberts S; Bellamy M; Curran SR; Sporikou CM; Bolton PF
    J Child Psychol Psychiatry; 2005 Oct; 46(10):1089-96. PubMed ID: 16178933
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Growth hormone secretion and its effect on height in pediatric patients with different genotypes of Prader-Willi syndrome.
    Oto Y; Obata K; Matsubara K; Kozu Y; Tsuchiya T; Sakazume S; Yoshino A; Murakami N; Ogata T; Nagai T
    Am J Med Genet A; 2012 Jun; 158A(6):1477-80. PubMed ID: 22585665
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.