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 *

103 related articles for article (PubMed ID: 3992159)

  • 41. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
    Destiné ML; Punnett HH; Thovichit S; DiGeorge AM; Weiss L
    Ann Genet; 1967 Jun; 10(2):65-9. PubMed ID: 5298975
    [No Abstract]   [Full Text] [Related]  

  • 42. [Trisomy 4p due to recombination aneusomy of an inversion 4 (p 14, q 35)].
    Rethoré MO; Dutrillaux B; Job JC; Lejeune J
    Ann Genet; 1974 Jun; 17(2):109-14. PubMed ID: 4547937
    [No Abstract]   [Full Text] [Related]  

  • 43. [Apropos of a translocation of a part of the long arms of a chromosome 5 on the long arms of a chromosome of the D group (Bq-, Dq+)].
    Beauvais P; Rumpler Y; Ruch JV; Dreyfus J; Haeberle C
    Arch Fr Pediatr; 1969; 26(6):695-704. PubMed ID: 5802061
    [No Abstract]   [Full Text] [Related]  

  • 44. Structural aberrations of chromosome 18. I. The 18p-syndrome.
    Schinzel A; Schmid W; Lüscher U; Nater M; Brook C; Steinmann B
    Arch Genet (Zur); 1974; 47(1):1-15. PubMed ID: 4469770
    [No Abstract]   [Full Text] [Related]  

  • 45. Autosomal chromosome aberrations in ophthalmology.
    Francois J
    Int Ophthalmol Clin; 1968; 8(4):839-910. PubMed ID: 4244691
    [No Abstract]   [Full Text] [Related]  

  • 46. Chromosome 4q deletion syndrome: a case report.
    Berger A; Dar H; Reiter A; Tal Y
    Isr J Med Sci; 1983 Sep; 19(9):850-2. PubMed ID: 6643027
    [No Abstract]   [Full Text] [Related]  

  • 47. Partial deletion of the short arm of a chromosome No. 4. Wolf's syndrome.
    van Kempen C; Jongbloet PH
    Maandschr Kindergeneeskd; 1967 Oct; 35(8):252-69. PubMed ID: 6065161
    [No Abstract]   [Full Text] [Related]  

  • 48. [A case of translocation t(Cp-; Bp+)].
    Ricci N; Ventimiglia B; Dallapiccola B; Preto G
    Ann Genet; 1967 Jun; 10(2):82-5. PubMed ID: 5298977
    [No Abstract]   [Full Text] [Related]  

  • 49. [The clinical importance of chromosome abnormalities. Some problems illustrated by 2 examples].
    Kristoffersen L; Howitz P; Nathan E; Lundsteen C
    Ugeskr Laeger; 1974 Jul; 136(29):1628-30. PubMed ID: 4844774
    [No Abstract]   [Full Text] [Related]  

  • 50. [Epilepsy in chromosome aberrations].
    Bahi-Buisson N; Ville D; Eisermann M; Plouin P; Kaminska A; Chiron C
    Arch Pediatr; 2005 Apr; 12(4):449-58. PubMed ID: 15808438
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Osseous malformations associated with chromosome abnormalities.
    Weiss L; Reynolds WA
    Orthop Clin North Am; 1972 Nov; 3(3):713-32. PubMed ID: 4264453
    [No Abstract]   [Full Text] [Related]  

  • 52. A taxonomic approach to the del(4p) phenotype.
    Preus M; Aymé S; Kaplan P; Vekemans M
    Am J Med Genet; 1985 Jun; 21(2):337-45. PubMed ID: 4014315
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Chromosomal mosaicism in the r (15) syndrome].
    Malygina NA; Mutovin GR; Filina NP; Akif'ev AP
    Genetika; 1980; 16(11):2029-33. PubMed ID: 7193157
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf-Hirschhorn syndrome.
    Flipsen-ten Berg K; van Hasselt PM; Eleveld MJ; van der Wijst SE; Hol FA; de Vroede MA; Beemer FA; Hochstenbach PF; Poot M
    Eur J Hum Genet; 2007 Nov; 15(11):1132-8. PubMed ID: 17637805
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat.
    Qumsiyeh MB; Stevens CA
    Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287
    [TBL] [Abstract][Full Text] [Related]  

  • 56. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22).
    Rivera H; Rivas F; Plascencia L; Cantú JM
    Ann Genet; 1983; 26(4):234-7. PubMed ID: 6607704
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Wolf-Hirschhorn syndrome with posterior intraorbital coloboma cyst: an unusual case.
    Tutunculer F; Acunas B; Hicdonmez T; Deviren A; Pelitli V
    Brain Dev; 2004 Apr; 26(3):203-5. PubMed ID: 15030910
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Prenatal diagnosis of interstitial deletion of 17(p11.2p11.2) (Smith-Magenis syndrome).
    Fan YS; Farrell SA
    Am J Med Genet; 1994 Jan; 49(2):253-4. PubMed ID: 8116679
    [No Abstract]   [Full Text] [Related]  

  • 59. Inverted duplication of 8p: ten new patients and review of the literature.
    Feldman GL; Weiss L; Phelan MC; Schroer RJ; Van Dyke DL
    Am J Med Genet; 1993 Sep; 47(4):482-6. PubMed ID: 8256810
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Subglottic pseudotumor, laryngeal dysplasia, and chondrodysplasia calcificans congenita with a t(D;B) chromosomal translocation.
    Valdmanis A; Wilson JR; Mann JD; Pearson G; Shaw MW
    Ann Genet; 1967 Jun; 10(2):55-9. PubMed ID: 5298973
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.