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 *

163 related articles for article (PubMed ID: 11355065)

  • 41. The oldest reported mirror hand? The curse of the coal-house frog!
    Marsden NJ; Whitaker IS; Boyce DE
    Ann R Coll Surg Engl; 2012 May; 94(4):e149-51. PubMed ID: 22613283
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Tricho-rhino-falangeal dysplasia type I. Giedion's syndrome].
    Nordshus T; Hagelsteen H
    Tidsskr Nor Laegeforen; 1980 Feb; 100(4):218-9. PubMed ID: 7376155
    [No Abstract]   [Full Text] [Related]  

  • 43. [The detection of congenital malformations of children's extremities].
    Raverdy E
    Soins Gynecol Obstet Pueric Pediatr; 1988 Mar; (82):9-10. PubMed ID: 3381178
    [No Abstract]   [Full Text] [Related]  

  • 44. [Coffin-Siris syndrome with Lennox-Gastaut syndrome and hypertrophic cardiomyopathy].
    Alembik Y; Roy E; Hirsch E; Tomb R; Stoll C
    Ann Pediatr (Paris); 1988 Sep; 35(7):491-4. PubMed ID: 3178112
    [No Abstract]   [Full Text] [Related]  

  • 45. Al-Awadi-Raas-Rothschild (limb/pelvis/uterus-hypoplasia/aplasia) syndrome and WNT7A mutations: genetic homogeneity and nosological delineation.
    Garavelli L; Wischmeijer A; Rosato S; Gelmini C; Reverberi S; Sassi S; Ferrari A; Mari F; Zabel B; Lausch E; Unger S; Superti-Furga A
    Am J Med Genet A; 2011 Feb; 155A(2):332-6. PubMed ID: 21271649
    [No Abstract]   [Full Text] [Related]  

  • 46. Anonychia and maxillofacial anomalies: an undefined syndrome?
    Copcu E; Sivrioglu N; Oztan Y
    Ann Plast Surg; 2006 Mar; 56(3):350-1. PubMed ID: 16508379
    [No Abstract]   [Full Text] [Related]  

  • 47. Costello syndrome and facio-cutaneous-skeletal syndrome.
    Philip N; Mancini J
    Am J Med Genet; 1993 Aug; 47(2):174-5. PubMed ID: 8213902
    [No Abstract]   [Full Text] [Related]  

  • 48. Hepatomegaly in a boy with ARID1B-related Coffin-Siris syndrome.
    Natsume T; Takano K; Motobayashi M; Kosho T
    Pediatr Int; 2018 Apr; 60(4):378-380. PubMed ID: 29504208
    [No Abstract]   [Full Text] [Related]  

  • 49. Pallister-Killian syndrome detected by fluorescence in situ hybridization.
    Bulter MG; Dev VG
    Am J Med Genet; 1995 Jul; 57(3):498-500. PubMed ID: 7677161
    [No Abstract]   [Full Text] [Related]  

  • 50. Autosomal recessive multiple pterygium syndrome: a new variant?
    Aslan Y; Erduran E; Kutlu N
    Am J Med Genet; 2000 Jul; 93(3):194-7. PubMed ID: 10925380
    [TBL] [Abstract][Full Text] [Related]  

  • 51. MR imaging in longitudinal epiphyseal bracket in children.
    Mahboubi S; Davidson R
    Pediatr Radiol; 1999 Apr; 29(4):259-61. PubMed ID: 10199903
    [No Abstract]   [Full Text] [Related]  

  • 52. Postaxial polydactyly.
    Aggarwal AN; Goyal MK; Rishi Gupta N
    JNMA J Nepal Med Assoc; 2009; 48(174):153-4. PubMed ID: 20387358
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [The cranio-carpo-tarsal dysplasia syndrome (the Freeman-Sheldon whistling-face syndrome). Practical significance of diagnosis].
    Kratzer W; Borm U
    Monatsschr Kinderheilkd (1902); 1978 May; 126(5):277-9. PubMed ID: 418327
    [No Abstract]   [Full Text] [Related]  

  • 54. A lethal syndrome of microcephaly with multiple congenital anomalies in three siblings.
    Neu RL; Kajii T; Gardner LI; Nagyfy SF
    Pediatrics; 1971 Mar; 47(3):610-2. PubMed ID: 5547878
    [No Abstract]   [Full Text] [Related]  

  • 55. Identical twins with mental retardation, dysarthria, progressive spastic paraplegia, and brachydactyly type E: a new syndrome or variant of Fitzsimmons-Guilbert syndrome?
    Lacassie Y; Arriaza MI; Duncan MC; Dijamco C; McElveen C; Stahls PF
    Am J Med Genet; 1999 May; 84(2):90-3. PubMed ID: 10323731
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Freeman-Sheldon syndrome with unusual hand and foot anomalies.
    Estrada R; Rosenfeld W; Salazar JD; Jhaveri R
    J Natl Med Assoc; 1981; 73(7):664-7. PubMed ID: 7265275
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Whistling face syndrome (Burian)].
    Rickhey B
    Z Orthop Ihre Grenzgeb; 1971 Jul; 109(3):532-4. PubMed ID: 4254815
    [No Abstract]   [Full Text] [Related]  

  • 58. Holoprosencephaly and split hand/foot: an additional case with this rare association.
    Abdel-Meguid N; Ashour AM
    Clin Dysmorphol; 2001 Oct; 10(4):277-9. PubMed ID: 11666003
    [No Abstract]   [Full Text] [Related]  

  • 59. Further delineation of a new (Van Den Ende-Gupta) syndrome of blepharophimosis contractural arachnodactyly, and characteristic face.
    Phadke SR; Gulati R; Agarwal SS
    Am J Med Genet; 1998 Apr; 77(1):16-8. PubMed ID: 9557887
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Prenatal diagnosis of hypoparathyroidism retardation and dysmorphism (HRD) syndrome.
    Hershkovitz E; Hershkovitz R; Hertzug L; Gorodischer R; Mazor M; Parvari R
    Prenat Diagn; 2000 Jun; 20(6):475-7. PubMed ID: 10861712
    [TBL] [Abstract][Full Text] [Related]  

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