BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

264 related articles for article (PubMed ID: 31964399)

  • 21. Cardiac rhabdomyoma as a possible new prenatal sonographic feature of Prader-Willi syndrome.
    Traisrisilp K; Sirikunalai P; Sirilert S; Chareonsirisuthigul T; Tongsong T
    J Obstet Gynaecol Res; 2022 Jan; 48(1):239-243. PubMed ID: 34655138
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Maternal age effect on the development of Prader-Willi syndrome resulting from upd(15)mat through meiosis 1 errors.
    Matsubara K; Murakami N; Nagai T; Ogata T
    J Hum Genet; 2011 Aug; 56(8):566-71. PubMed ID: 21633360
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Risk assessment of medically assisted reproduction and advanced maternal ages in the development of Prader-Willi syndrome due to UPD(15)mat.
    Matsubara K; Murakami N; Fukami M; Kagami M; Nagai T; Ogata T
    Clin Genet; 2016 May; 89(5):614-9. PubMed ID: 26526156
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mosaic maternal uniparental disomy of chromosome 15 in Prader-Willi syndrome: utility of genome-wide SNP array.
    Izumi K; Santani AB; Deardorff MA; Feret HA; Tischler T; Thiel BD; Mulchandani S; Stolle CA; Spinner NB; Zackai EH; Conlin LK
    Am J Med Genet A; 2013 Jan; 161A(1):166-71. PubMed ID: 23225330
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Neonatal presentation of Prader-Willi syndrome: A report of five cases].
    Richard-De Ceaurriz B; Leymarie C; Godefroy A; Collignon P; Sigaudy S; Truc P
    Arch Pediatr; 2017 Nov; 24(11):1115-1120. PubMed ID: 28967604
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Prader-Willi syndrome--a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders.
    Veltman MW; Thompson RJ; Roberts SE; Thomas NS; Whittington J; Bolton PF
    Eur Child Adolesc Psychiatry; 2004 Feb; 13(1):42-50. PubMed ID: 14991431
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Complex rearrangements of chromosome 15 in two patients with mild/atypical Prader Willi syndrome.
    Salavoura K; Kolialexi A; Sofocleous C; Kalaitzidaki M; Pampanos A; Kitsiou S; Mavrou A
    Genet Couns; 2008; 19(2):219-24. PubMed ID: 18618997
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15.
    L'Herminé AC; Aboura A; Brisset S; Cuisset L; Castaigne V; Labrune P; Frydman R; Tachdjian G
    Prenat Diagn; 2003 Nov; 23(11):938-43. PubMed ID: 14634983
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Brain-stem serotonin transporter availability in maternal uniparental disomy and deletion Prader-Willi syndrome.
    Krishnadas R; Cooper SA; Nicol A; Pimlott S; Soni S; Holland AJ; McArthur L; Cavanagh J
    Br J Psychiatry; 2018 Jan; 212(1):57-58. PubMed ID: 29433608
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Changing rates of genetic subtypes of Prader-Willi syndrome in the UK.
    Whittington JE; Butler JV; Holland AJ
    Eur J Hum Genet; 2007 Jan; 15(1):127-30. PubMed ID: 16957680
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Maternal uniparental disomy 14; differential diagnosis with Prader-Willi syndrome].
    Tamminga S; Stalman SE; Kamp GA; Hendriks YM; Knegt AC; Elting MW
    Ned Tijdschr Geneeskd; 2015; 159():A8240. PubMed ID: 25898865
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Impact of genetic subtypes of Prader-Willi syndrome with growth hormone therapy on intelligence and body mass index.
    Butler MG; Matthews NA; Patel N; Surampalli A; Gold JA; Khare M; Thompson T; Cassidy SB; Kimonis VE
    Am J Med Genet A; 2019 Sep; 179(9):1826-1835. PubMed ID: 31313492
    [TBL] [Abstract][Full Text] [Related]  

  • 36. X-chromosome inactivation patterns in females with Prader-Willi syndrome.
    Butler MG; Theodoro MF; Bittel DC; Kuipers PJ; Driscoll DJ; Talebizadeh Z
    Am J Med Genet A; 2007 Mar; 143A(5):469-75. PubMed ID: 17036338
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The proportion of uniparental disomy is increased in Prader-Willi syndrome due to an advanced maternal childbearing age in Korea.
    Cho SY; Ki CS; Sohn YB; Maeng SH; Jung YJ; Kim SJ; Jin DK
    J Hum Genet; 2013 Mar; 58(3):150-4. PubMed ID: 23303386
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation-specific PCR.
    Mitter D; Buiting K; von Eggeling F; Kuechler A; Liehr T; Mau-Holzmann UA; Prott EC; Wieczorek D; Gillessen-Kaesbach G
    Am J Med Genet A; 2006 Oct; 140(19):2039-49. PubMed ID: 16906536
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Prenatal diagnosis of Prader-Willi syndrome due to uniparental disomy with NIPS: Case report and literature review.
    Shubina J; Barkov IY; Stupko OK; Kuznetsova MV; Goltsov AY; Kochetkova TO; Trofimov DY; Sukhikh GT
    Mol Genet Genomic Med; 2020 Oct; 8(10):e1448. PubMed ID: 32857485
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.