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 *

68 related articles for article (PubMed ID: 1218204)

  • 21. [Families with recurrent cases of Waardenburg-Klein syndrome].
    Bliumina MG; Moskovkina AG
    Genetika; 1985 Jun; 21(6):1062-5. PubMed ID: 4029612
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Cri-du-chat syndrome and two other deformed children in a family carrying a pericentric inversion or insertion of chromosome 5].
    Delozier-Blanchet CD; Pitmon D; Schorderet D; Engel E
    J Genet Hum; 1985 Dec; 33(5):371-80. PubMed ID: 4093767
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Tricho-dento-osseous syndrome: heterogeneity or clinical variability.
    Shapiro SD; Quattromani FL; Jorgenson RJ; Young RS
    Am J Med Genet; 1983 Oct; 16(2):225-36. PubMed ID: 6650567
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Congenital absence of the patella: two cases reported].
    Ly-Ba A; Ndao AK; Ba-Diop S; Ly-N'Diaye F; Ndiaye AR; Ndoye Diop A; Gueye B; M'Bengue A; Badiane M
    Mali Med; 2008; 23(1):57-60. PubMed ID: 19437818
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Autosomal dominant inheritance of the Aarskog syndrome.
    Grier RE; Farrington FH; Kendig R; Mamunes P
    Am J Med Genet; 1983 May; 15(1):39-46. PubMed ID: 6344635
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genitopatellar syndrome: a recognizable phenotype.
    Reardon W
    Am J Med Genet; 2002 Aug; 111(3):313-5. PubMed ID: 12210329
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Van Der Woude syndrome: variable penetrance of a novel mutation (p.Arg 84Gly) of the IRF6 gene in a Turkish family.
    Item CB; Turhani D; Thurnher D; Yerit K; Sinko K; Wittwer G; Adeyemo WL; Frei K; Erginel-Unaltuna N; Watzinger F; Ewers R
    Int J Mol Med; 2005 Feb; 15(2):247-51. PubMed ID: 15647839
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12.
    Bonnet D; Pelet A; Legeai-Mallet L; Sidi D; Mathieu M; Parent P; Plauchu H; Serville F; Schinzel A; Weissenbach J
    Nat Genet; 1994 Apr; 6(4):405-8. PubMed ID: 8054983
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Another adult with Meier-Gorlin syndrome--insights into the natural history.
    Shalev SA; Hall JG
    Clin Dysmorphol; 2003 Jul; 12(3):167-9. PubMed ID: 14564153
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Congenital aplasia of the patella and the distal third of the quadriceps mechanism.
    Varghese RA; Joseph B
    J Pediatr Orthop B; 2007 Sep; 16(5):323-6. PubMed ID: 17762670
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Meier-Gorlin syndrome: report of eight additional cases and review.
    Bongers EM; Opitz JM; Fryer A; Sarda P; Hennekam RC; Hall BD; Superneau DW; Harbison M; Poss A; van Bokhoven H; Hamel BC; Knoers NV
    Am J Med Genet; 2001 Aug; 102(2):115-24. PubMed ID: 11477602
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Congenital patellar syndrome.
    Jerome JT; Varghese M; Sankaran B
    Rom J Morphol Embryol; 2009; 50(2):291-3. PubMed ID: 19434325
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Inherited partial aniridia, microcornea with high myopia and Bergmeister's papilla: a new phenotypic expression.
    Naithani P; Sinha A; Gupta V
    Indian J Ophthalmol; 2008; 56(2):145-6. PubMed ID: 18292626
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Familial aplasia or hypoplasia of the patella.
    Braun HS
    Clin Genet; 1978 Apr; 13(4):350-2. PubMed ID: 657574
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Ischio-pubic-patellar hypoplasia: is it a new syndrome?
    Habboub HK; Thneibat WA
    Pediatr Radiol; 1997 May; 27(5):430-1. PubMed ID: 9133357
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Evidence for genetic heterogeneity in familial isolated patella aplasia-hypoplasia.
    Bongers EM; van Bokhoven H; Knoers NV; Hamel BC; Woods CG
    Am J Med Genet; 2002 Feb; 108(1):78-9. PubMed ID: 11857555
    [No Abstract]   [Full Text] [Related]  

  • 37. [A rare case of absence of the patellae].
    Durbanov IM
    Khirurgiia (Mosk); 1992; (7-8):88. PubMed ID: 1469883
    [No Abstract]   [Full Text] [Related]  

  • 38. Recurrent dislocation of the patella versus generalized joint laxity.
    Shapiro SD; Jorgenson RJ; Salinas CF
    Birth Defects Orig Artic Ser; 1976; 12(5):287-91. PubMed ID: 953233
    [No Abstract]   [Full Text] [Related]  

  • 39. A new patella syndrome.
    Sandhaus YS; Ben-Ami T; Chechick A; Goodman RM
    Clin Genet; 1987 Mar; 31(3):143-7. PubMed ID: 3568440
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genitopatellar syndrome: a further case.
    Brugha R; Kinali M; Aminu K; Bridges N; Holder SE
    Clin Dysmorphol; 2011 Jul; 20(3):163-165. PubMed ID: 21412151
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.