BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

87 related articles for article (PubMed ID: 3216192)

  • 21. The hydrolethalus syndrome.
    Krassikoff N; Konick L; Gilbert EF
    Birth Defects Orig Artic Ser; 1987; 23(1):411-9. PubMed ID: 3580557
    [No Abstract]   [Full Text] [Related]  

  • 22. Holt-Oram syndrome with polydactyly and ostium primum defect.
    Kejariwal VK; Misra PK; Kumar A; Awasthi S
    Indian Pediatr; 1989 Oct; 26(10):1064-5. PubMed ID: 2630456
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. Picture of the month. Short-rib polydactyly dwarfism: Saldino-Noonan type.
    Kataria S; Kushnick T
    Am J Dis Child; 1982 Jul; 136(7):639-40. PubMed ID: 7091096
    [No Abstract]   [Full Text] [Related]  

  • 25. Goldenhar's syndrome associated with multiple congenital abnormalities.
    Bayraktar S; Bayraktar ST; Ataoglu E; Ayaz A; Elevli M
    J Trop Pediatr; 2005 Dec; 51(6):377-9. PubMed ID: 16186139
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Polysyndactyly with complex cardiopathy. Apropos of 3 cases in the same family].
    Bonneau JC; Moirot H; Bastard C; Petitcolas J; Ropartz C
    J Genet Hum; 1983 Jun; 31(2):93-105. PubMed ID: 6313864
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Hydrolethalus syndrome].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 Jan; 14(1):35-6. PubMed ID: 8451226
    [No Abstract]   [Full Text] [Related]  

  • 28. Six patients with oral-facial-digital syndrome IV: the case for heterogeneity.
    Toriello HV; Carey JC; Suslak E; Desposito FR; Leonard B; Lipson M; Friedman BD; Hoyme HE
    Am J Med Genet; 1997 Mar; 69(3):250-60. PubMed ID: 9096753
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Atrioventricular septal defect associated with type A postaxial polydactyly.
    Levin SE; Vanderdonck K
    Cardiol Young; 2004 Apr; 14(2):215-8. PubMed ID: 15691417
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The Pena-Shokeir syndrome: report of nine Dutch cases.
    Lindhout D; Hageman G; Beemer FA; Ippel PF; Breslau-Siderius L; Willemse J
    Am J Med Genet; 1985 Aug; 21(4):655-68. PubMed ID: 3895932
    [TBL] [Abstract][Full Text] [Related]  

  • 31. OEIS complex with major cardiac malformation: a case report.
    Batra P; Saha A; Vilhekar KY; Gupta A
    Indian J Pathol Microbiol; 2007 Apr; 50(2):365-6. PubMed ID: 17883075
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Post-axial polydactyly-progressive myopia syndrome of dominant heredity].
    Czeizel E; Brooser G
    Orv Hetil; 1986 Feb; 127(8):453-4, 457. PubMed ID: 2869465
    [No Abstract]   [Full Text] [Related]  

  • 33. Syndromal hypothalamic hamartoblastoma with holoprosencephaly sequence, microphthalmia, pulmonary malformations, radial hypoplasia and müllerian regression: further delineation of a new syndrome?
    Verloes A; Narcy F; Fallet-Bianco C
    Clin Dysmorphol; 1995 Jan; 4(1):33-7. PubMed ID: 7735503
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Hydrolethalus syndrome: neuropathology of 21 cases confirmed by HYLS1 gene mutation analysis.
    Paetau A; Honkala H; Salonen R; Ignatius J; Kestilä M; Herva R
    J Neuropathol Exp Neurol; 2008 Aug; 67(8):750-62. PubMed ID: 18648327
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Goldenhar syndrome. Report of a new case].
    Pedraz García C; Benito Zaballos MF; García González P; Carbajosa Herrero T; Heras de Pedro M; Santos Borbujo J; Gil Sánchez A; Salazar Villalobos V
    An Esp Pediatr; 1984 Mar; 20(4):403-7. PubMed ID: 6732067
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Steinfeld syndrome: report of a second family and further delineation of a rare autosomal dominant disorder.
    Nöthen MM; Knöpfle G; Födisch HJ; Zerres K
    Am J Med Genet; 1993 Jun; 46(4):467-70. PubMed ID: 8357025
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Diaphragmatic hernia in the Coffin-Siris syndrome.
    Delvaux V; Moerman P; Fryns JP
    Genet Couns; 1998; 9(1):45-50. PubMed ID: 9555587
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A syndrome of brachyphalangy, polydactyly and absent tibiae.
    Baraitser M; Stewart F; Winter RM; Hall CM; Herman S; Nevin NC
    Clin Dysmorphol; 1997 Apr; 6(2):111-21. PubMed ID: 9134290
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Cerebellar hypoplasia, facial dysmorphism and internal abnormalities: a new recessive syndrome?
    Seller MJ; Pal K; Moscoso G; Nicolaides K; Hyett JA
    Clin Dysmorphol; 1998 Jan; 7(1):41-4. PubMed ID: 9546829
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Peripheral neuropathy in cardiofaciocutaneous syndrome.
    DeRoos ST; Ryan MM; Ouvrier RA
    Pediatr Neurol; 2007 Apr; 36(4):250-2. PubMed ID: 17437909
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.