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 *

170 related articles for article (PubMed ID: 31270759)

  • 21. Multicentre study of maternal and neonatal outcomes in individuals with Prader-Willi syndrome.
    Singh P; Mahmoud R; Gold JA; Miller JL; Roof E; Tamura R; Dykens E; Butler MG; Driscoll DJ; Kimonis V
    J Med Genet; 2018 Sep; 55(9):594-598. PubMed ID: 29776967
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. Maternal uniparental disomy in a patient with Prader-Willi syndrome with an additional small inv dup(15) chromosome.
    Wang YM; Chuang L; Wang BT; Kuo PL
    J Formos Med Assoc; 2004 Dec; 103(12):943-7. PubMed ID: 15624046
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prader-Willi-like phenotypes: a systematic review of their chromosomal abnormalities.
    Rocha CF; Paiva CL
    Genet Mol Res; 2014 Mar; 13(1):2290-8. PubMed ID: 24737477
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Small mosaic deletion encompassing the snoRNAs and SNURF-SNRPN results in an atypical Prader-Willi syndrome phenotype.
    Anderlid BM; Lundin J; Malmgren H; Lehtihet M; Nordgren A
    Am J Med Genet A; 2014 Feb; 164A(2):425-31. PubMed ID: 24311433
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Grey matter volume and cortical structure in Prader-Willi syndrome compared to typically developing young adults.
    Manning KE; Tait R; Suckling J; Holland AJ
    Neuroimage Clin; 2018; 17():899-909. PubMed ID: 29527494
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Differences in behavioural phenotype between parental deletion and maternal uniparental disomy in Prader-Willi syndrome: an ERP study.
    Stauder JE; Boer H; Gerits RH; Tummers A; Whittington J; Curfs LM
    Clin Neurophysiol; 2005 Jun; 116(6):1464-70. PubMed ID: 15978509
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Increased brain age in adults with Prader-Willi syndrome.
    Azor AM; Cole JH; Holland AJ; Dumba M; Patel MC; Sadlon A; Goldstone AP; Manning KE
    Neuroimage Clin; 2019; 21():101664. PubMed ID: 30658944
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The Spectrum of the Prader-Willi-like Pheno- and Genotype: A Review of the Literature.
    Juriaans AF; Kerkhof GF; Hokken-Koelega ACS
    Endocr Rev; 2022 Jan; 43(1):1-18. PubMed ID: 34460908
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome.
    Duker AL; Ballif BC; Bawle EV; Person RE; Mahadevan S; Alliman S; Thompson R; Traylor R; Bejjani BA; Shaffer LG; Rosenfeld JA; Lamb AN; Sahoo T
    Eur J Hum Genet; 2010 Nov; 18(11):1196-201. PubMed ID: 20588305
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defects.
    Hassan M; Butler MG
    Eur J Med Genet; 2016 Nov; 59(11):584-589. PubMed ID: 27659713
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adults.
    Manzardo AM; Weisensel N; Ayala S; Hossain W; Butler MG
    Clin Genet; 2018 Mar; 93(3):622-631. PubMed ID: 28984907
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prevalence of Prader-Willi syndrome among infants with hypotonia.
    Tuysuz B; Kartal N; Erener-Ercan T; Guclu-Geyik F; Vural M; Perk Y; Erçal D; Erginel-Unaltuna N
    J Pediatr; 2014 May; 164(5):1064-7. PubMed ID: 24582009
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. 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]  

  • 38. Prader-Willi syndrome: genetic tests and clinical findings.
    Fridman C; Varela MC; Kok F; Setian N; Koiffmann CP
    Genet Test; 2000; 4(4):387-92. PubMed ID: 11216664
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Investigating the correlation between genotype and phenotype in Prader-Willi syndrome: a study of 45 cases from Brazil.
    Cintra HA; Rocha DN; da Costa ACC; Tyszler LS; Freitas S; de Araujo LA; Crozoe LI; de Paula LR; Correia PS; Gomes LHF; da Cunha Guida L
    Orphanet J Rare Dis; 2024 Jun; 19(1):240. PubMed ID: 38902749
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Effectiveness of multiplex ligation-dependent probe amplification assay used for detecting deletion of Prader-Willi syndrome.
    Shao H; Lip V; Wu BL
    Beijing Da Xue Xue Bao Yi Xue Ban; 2005 Feb; 37(1):64-7. PubMed ID: 15719045
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.