BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 25434475)

  • 1. A rare case of 3C disease: Ritscher-Schinzel syndrome presenting with recurrent talipes equinovarus.
    Konya MN; Elmas M; Erginoğlu SE; Yeşil M
    Int J Surg Case Rep; 2015; 7C():130-3. PubMed ID: 25434475
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
    Leonardi ML; Pai GS; Wilkes B; Lebel RR
    Am J Med Genet; 2001 Aug; 102(3):237-42. PubMed ID: 11484200
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [A phenotypic description of 26 patients with Ritscher-Schinzel syndrome (cranio-cerebello-cardiac dysplasia or 3C syndrome)].
    Pira-Paredes SM; Montoya-Villada JH; Franco-Restrepo JL; Moncada-Velez M; Cornejo JW
    Rev Neurol; 2017 Jun; 64(11):481-488. PubMed ID: 28555453
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A preterm infant with prolonged respiratory problems due to Ritscher-Schinzel syndrome.
    Yurttutan S; Oncel MY; Yurttutan N; Altug N; Erdeve O; Dilmen U
    Genet Couns; 2012; 23(3):383-7. PubMed ID: 23072186
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ritscher-Schinzel (cranio-cerebello-cardiac, 3C) syndrome: report of four new cases with renal involvement.
    Seidahmed MZ; Alkuraya FS; Shaheed M; Al Zahrani M; Al Manea W; Mansour F; Mustafa T; Farid G; Salih MA
    Am J Med Genet A; 2011 Jun; 155A(6):1393-7. PubMed ID: 21567916
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ritscher-Schinzel (3C) syndrome: documentation of the phenotype.
    Kosaki K; Curry CJ; Roeder E; Jones KL
    Am J Med Genet; 1997 Feb; 68(4):421-7. PubMed ID: 9021015
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Biallelic VPS35L pathogenic variants cause 3C/Ritscher-Schinzel-like syndrome through dysfunction of retriever complex.
    Kato K; Oka Y; Muramatsu H; Vasilev FF; Otomo T; Oishi H; Kawano Y; Kidokoro H; Nakazawa Y; Ogi T; Takahashi Y; Saitoh S
    J Med Genet; 2020 Apr; 57(4):245-253. PubMed ID: 31712251
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sibs with Ritscher-Schinzel (3C) syndrome and anal malformations.
    Orstavik KH; Bechensteen AG; Fugelseth D; Orderud W
    Am J Med Genet; 1998 Jan; 75(3):300-3. PubMed ID: 9475602
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expansion of the CCDC22 associated Ritscher-Schinzel/3C syndrome and review of the literature: Should the minimal diagnostic criteria be revised?
    Gjerulfsen CE; Møller RS; Fenger CD; Hammer TB; Bayat A
    Eur J Med Genet; 2021 Jul; 64(7):104246. PubMed ID: 34020006
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 3C syndrome: third occurrence of cranio-cerebello-cardiac dysplasia (Ritscher-Schinzel syndrome).
    Verloes A; Dresse MF; Jovanovic M; Dodinval P; Geubelle F
    Clin Genet; 1989 Mar; 35(3):205-8. PubMed ID: 2650935
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 3C syndrome with cryptorchidism and posterior embryotoxon.
    Papadopoulou E; Sifakis S; Rogalidou M; Makrigiannakis A; Giannakopoulou C; Petersen MB
    Clin Dysmorphol; 2005 Apr; 14(2):97-100. PubMed ID: 15770133
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Delineating the CCDC22-related Ritscher-Schinzel syndrome phenotype in the original family.
    Rodgers J; Richmond CM; McGaughran J
    Am J Med Genet A; 2022 Nov; 188(11):3324-3330. PubMed ID: 36073196
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cranio-cerebello-cardiac (3C) syndrome: follow-up study of the original patient.
    Zankl A; Güngör T; Schinzel A
    Am J Med Genet A; 2003 Apr; 118A(1):55-9. PubMed ID: 12605442
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ritscher-Schinzel cranio-cerebello-cardiac syndrome.
    Herman TE; Siegel MJ
    J Perinatol; 2008 Oct; 28(10):715-8. PubMed ID: 18825150
    [No Abstract]   [Full Text] [Related]  

  • 15. Another case of Ritscher-Schinzel-syndrome: craniocerebello-cardiac dysplasia (3C-syndrome) with associated bilateral colobomata.
    Wörle H; Lewin MA; Holder M; Bastanier CK; Köhler B
    Eur J Pediatr; 1994 Feb; 153(2):140. PubMed ID: 8157023
    [No Abstract]   [Full Text] [Related]  

  • 16. Expanding the pre- and postnatal phenotype of WASHC5 and CCDC22 -related Ritscher-Schinzel syndromes.
    Neri S; Maia N; Fortuna AM; Damasio J; Coale E; Willis M; Jorge P; Højte AF; Fenger CD; Møller RS; Bayat A
    Eur J Med Genet; 2022 Nov; 65(11):104624. PubMed ID: 36130690
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Ritscher-Schinzel syndrome caused by CCDC22 gene mutation: a case report].
    Liang YT; Jiang HY; Fu HY
    Zhongguo Dang Dai Er Ke Za Zhi; 2020 Oct; 22(10):1135-1137. PubMed ID: 33059814
    [TBL] [Abstract][Full Text] [Related]  

  • 18. "Shifted" threshold may explain diversity of cardiovascular malformations in multiple congenital abnormalities syndromes: 3C (Ritscher-Schinzel) syndrome as an example.
    Lurie IW; Ferencz C
    Am J Med Genet; 1996 Dec; 66(1):72-4. PubMed ID: 8957516
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Radiographic characterization of the hands in Ritscher-Schinzel/3-C syndrome.
    Friesen KJ; Chodirker BN; Chudley AE; Reed MH; Elliott AM
    Springerplus; 2013; 2():594. PubMed ID: 24255872
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.