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 *

273 related articles for article (PubMed ID: 316677)

  • 21. Trisomy 14 mosaicism in a liveborn male: clinical report and review of the literature.
    Kaplan LC; Wayne A; Crowell S; Latt SA
    Am J Med Genet; 1986 Apr; 23(4):925-30. PubMed ID: 3515939
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The 12p trisomy syndrome.
    Armendares S; Salamanca F; Nava S; Ramirez S; Cantu JM
    Ann Genet; 1975 Jun; 18(2):89-94. PubMed ID: 1081370
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22).
    Bowen P; Fitzgerald PH; Gardner RJ; Biederman B; Veale AM
    Am J Med Genet; 1983 Apr; 14(4):635-46. PubMed ID: 6846399
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development.
    Ausems MG; Van Spijker HG; Dijkhuis HJ; Swanenburg De Veye HF; Bijlsma JB
    Genet Couns; 1996; 7(1):61-5. PubMed ID: 8652090
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mosaic trisomy 9 syndrome with unusual phenotype.
    Kaminker CP; Daín L; Lamas MA; Sánchez JM
    Am J Med Genet; 1985 Oct; 22(2):237-41. PubMed ID: 3931476
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Unilateral microtia in an infant with trisomy 18 mosaicism.
    Giannatou E; Leze H; Katana A; Kolialexi A; Mavrou A; Kanavakis E; Kitsiou-Tzeli S
    Genet Couns; 2009; 20(2):181-7. PubMed ID: 19650416
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Duplication 12q mosaicism in two unrelated patients with a similar syndrome.
    Harrod MJ; Byrne JB; Dev VG; Francke U
    Am J Med Genet; 1980; 7(2):123-9. PubMed ID: 7468644
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Long arm deletion of chromosome 13 with exclusion of esterase D from 13q32 leads to 13qter.
    Telfer MA; Clark CE; Casey PA; Cowell HR; Stroud HH
    Clin Genet; 1980 Jun; 17(6):428-32. PubMed ID: 7398115
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype.
    Fryns JP; Kleczkowska A; Kenis H; Decock P; Van den Berghe H
    Ann Genet; 1989; 32(3):174-6. PubMed ID: 2573314
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)].
    Raoul O; Rethoré MO; Dutriliaux B; Michon L; Lejeune J
    Ann Genet; 1975 Mar; 18(1):35-9. PubMed ID: 1080036
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Skin pigment anomalies and mosaicism for a double autosomal trisomy (48,XX,+18,+20).
    Devriendt K; Matthijs G; Meireleire J; Roelen L; van Buggenhout G; Fryns JP
    Genet Couns; 1998; 9(4):283-6. PubMed ID: 9894166
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Trisomy 6q25 leads to 6qter in two sisters resulting from maternal 6;11 translocation.
    Clark CE; Cowell HR; Telfer MA; Casey PA
    Am J Med Genet; 1980; 5(2):171-8. PubMed ID: 7395910
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [A new case of trisomy 5p].
    Antonenko VG; Levina LIa; Chudnova VI
    Genetika; 1985 Dec; 21(12):2066-70. PubMed ID: 4085794
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Complementary duplication and deletion of 17 (pcen----p11.2): a family with a supernumerary chromosome comprised of an interstitially deleted segment.
    Friedman JM; Harrod MJ; Howard-Peebles PN
    Am J Med Genet; 1992 Sep; 44(1):37-40. PubMed ID: 1519647
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Trisomy 9 mosaicism in a girl with multiple malformations.
    Diaz-Mares L; Molina B; Carnevale A
    Ann Genet; 1990; 33(3):165-8. PubMed ID: 2288462
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Familial translocation 3/22 MAT with partial trisomy 3q (author's transl)].
    Schwanitz G; Schmid RD; Grosse G; Grahn-Liebe E
    J Genet Hum; 1977 Jun; 25(2):141-50. PubMed ID: 556338
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 46,X,i(Xq)/47,XX,+13 mosaicism.
    Igarashi M; Tsukahara M; Sugio Y; Katayama K; Kajii T
    Ann Genet; 1985; 28(4):241-4. PubMed ID: 3879438
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18].
    Vivarelli R; Paolieri M; Anichini C; Scarinci R; Berardi R; Rosaia L; Pucci L
    Boll Soc Ital Biol Sper; 1992 Apr; 68(4):263-9. PubMed ID: 1463601
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Trisomy 14 mosaicism: case report and review.
    Johnson VP; Aceto T; Likness C
    Am J Med Genet; 1979; 3(4):331-9. PubMed ID: 474633
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 46,XX,-12,+der(12),rcp(3;12)(p25.1;p13.31)pat karyotype in a girl. Probable subregional assignment of glyceraldehyde-3-phosphate dehydrogenase locus to 12p13.1----p13.31 by exclusion mapping.
    Rivas F; Vaca G; Zúñiga G; González RM; Ruiz C; Rivera H; Moller M; Cantu JM
    Ann Genet; 1985; 28(3):189-92. PubMed ID: 3879156
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.