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 *

95 related articles for article (PubMed ID: 8350593)

  • 21. Hormonal versus genetic factors in limb and heart anomalies.
    el-Gindi E; Ahmed-Nasr M
    Cardiovasc Surg; 1993 Aug; 1(4):381-3. PubMed ID: 8076064
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A dysmorphic newborn infant with a complex rearrangement involving chromosomes 2, 4, and 6 detected by fluorescence in situ hybridization (FISH).
    Hoffman DJ; Punnett HH; Pyeritz RE
    Am J Perinatol; 2004 Feb; 21(2):69-71. PubMed ID: 15017469
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Aminopterin-like syndrome sine aminopterin associated with translocation involving chromosomes 5 and 10.
    Chen MF; Vekemans M; Meagher-Villemure K; Outerbridge E; Fraser FC; Der Kaloustian VM
    Am J Med Genet; 1990 Dec; 37(4):478-81. PubMed ID: 2260592
    [TBL] [Abstract][Full Text] [Related]  

  • 24. De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome.
    Chitayat D; Fagerstrom CL; Kalousek DK; Rootman J; Taylor GP; Hall JG
    Am J Med Genet; 1989 Jan; 32(1):36-41. PubMed ID: 2495721
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The WT syndrome--a "new" autosomal dominant pleiotropic trait of radial/ulnar hypoplasia with high risk of bone marrow failure and/or leukemia.
    Gonzalez CH; Durkin-Stamm MV; Geimer NF; Shahidi NT; Schilling RF; Rubira F; Opitz JM
    Birth Defects Orig Artic Ser; 1977; 13(3B):31-8. PubMed ID: 890097
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
    Shaffer LG; Spikes AS; Macha M; Dunn R
    J Reprod Med; 1996 May; 41(5):367-71. PubMed ID: 8725766
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Clinical variability of partial duplication 1q: a clinical report and literature review.
    Rosenthal J; Abeliovich D; Carmi R
    Am J Med Genet; 1987 Aug; 27(4):787-92. PubMed ID: 3122569
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Ulnar ray defect in an infant with a 6q21;7q31.2 translocation: further evidence for the existence of a limb defect gene in 6q21.
    Gurrieri F; Cammarata M; Avarello RM; Genuardi M; Pomponi MG; Neri G; Giuffrè L
    Am J Med Genet; 1995 Jan; 55(3):315-8. PubMed ID: 7726229
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Rieger syndrome with de novo reciprocal translocation t(1;4) (q23.1;q25).
    Makita Y; Masuno M; Imaizumi K; Yamashita S; Ohba S; Ito D; Kuroki Y
    Am J Med Genet; 1995 May; 57(1):19-21. PubMed ID: 7645592
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Apical hypertrophic cardiomyopathy and atrial septal defect: part of a multi-organ syndrome?
    Pattoneri P; Pelà G; Astorri E; Borghetti A
    Eur J Echocardiogr; 2007 Jun; 8(3):226-9. PubMed ID: 16542879
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Deformities of the extremities in Holt-Oram syndrome].
    Hupfauer W; Seling A
    Z Orthop Ihre Grenzgeb; 1971 May; 109(2):270-6. PubMed ID: 4254058
    [No Abstract]   [Full Text] [Related]  

  • 32. 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]  

  • 33. [Variants of radial hemimelia with and without vitium cordis (Holt-Oram syndrome) in 2 families].
    Pfeiffer RA; Böwing B; Deeg KH
    Monatsschr Kinderheilkd; 1989 May; 137(5):275-9. PubMed ID: 2739665
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Holt-Oram syndrome with right lung agenesis caused by a de novo mutation in the TBX5 gene.
    Tseng YR; Su YN; Lu FL; Jeng SF; Hsieh WS; Chen CY; Chou HC; Peng SS
    Am J Med Genet A; 2007 May; 143A(9):1012-4. PubMed ID: 17366586
    [No Abstract]   [Full Text] [Related]  

  • 35. Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome.
    Wheeler PG; Weaver DD; Palmer CG
    Am J Med Genet; 1995 Feb; 55(4):462-5. PubMed ID: 7762587
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [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]  

  • 37. [Report of a family with Holt-Oram syndrome (author's transl)].
    Gaul G; Titscher G; Brand O; Heeger H
    Z Kardiol; 1979 Mar; 68(3):173-5. PubMed ID: 442759
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Duplication 11q and deletion 5p syndromes due to a reciprocal translocation segregating in four generations.
    Mutchinick O; Ramos Z; Sánchez F; Ruz L; Lisker R; Ovseyevitz J
    Am J Med Genet; 1988 Jan; 29(1):187-92. PubMed ID: 3344767
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Newborn with phocomelia and thrombocytopenia. Case report].
    Maas C; Arand J; Orlikowsky T; Goelz R
    Z Geburtshilfe Neonatol; 2002; 206(4):161-3. PubMed ID: 12198594
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 8q22-->qter duplication in a child with multiple congenital malformations: case report.
    Sasiadek M; Stembalska A; Schlade K; Zych M
    Med Sci Monit; 2000; 6(1):141-4. PubMed ID: 11208302
    [TBL] [Abstract][Full Text] [Related]  

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