BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 4240724)

  • 1. 46,XY,21qi-46,XY,21p- mosaicism in a child with Down's syndrome.
    Atkins L; Feingold M
    J Med Genet; 1969 Jun; 6(2):206-8. PubMed ID: 4240724
    [No Abstract]   [Full Text] [Related]  

  • 2. Dissociation as probable origin of mosaic 45,XY,t(15;21)/46,XY,i(21q).
    Vianna-Morgante AM; Nunesmaia HG
    J Med Genet; 1978 Aug; 15(4):305-10. PubMed ID: 152355
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Down's syndrome associated with two Robertsonian translocations, 45,XX,-15,-21, + t(15q21q) and 46,XX,-21, + t(21q21q).
    Atkins L; Bartsocas CS
    J Med Genet; 1974 Sep; 11(3):306-9. PubMed ID: 4279290
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Karyotypic analysis of 150 cases of Down's Syndrome in Iraq.
    Ferman A; Shakir A
    J Ment Defic Res; 1976 Jun; 20(2):83-7. PubMed ID: 133247
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Down's syndrome transmitted through maternal mosaicism.
    Aarskog D
    Acta Paediatr Scand; 1969 Nov; 58(6):609-14. PubMed ID: 4244880
    [No Abstract]   [Full Text] [Related]  

  • 6. [Complete Down's syndrome in a boy, formed by chromosomic mosaicism 46-XY isochromosome 21 and 47-XY, trisomy 21 with mosaicism of the mother 46-XX and 47-XX, trisomy 21)].
    Raichs A; Tamparillas M
    Sangre (Barc); 1967; 12(1):71-80. PubMed ID: 4235850
    [No Abstract]   [Full Text] [Related]  

  • 7. De novo translocation Down's syndrome: risk of recurrence of Down's syndrome.
    Gardner RJ; Veale AM
    Clin Genet; 1974; 6(3):160-4. PubMed ID: 4279152
    [No Abstract]   [Full Text] [Related]  

  • 8. Reciprocal translocation, 4q-; 21p+, giving rise to Down's syndrome.
    Jenkins MB; Boyd L
    J Med Genet; 1976 Aug; 13(4):323-6. PubMed ID: 134161
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Clinical symptoms of Down's syndrome and its variations].
    Seidlitz G
    Padiatr Grenzgeb; 1974; 13(4):205-17. PubMed ID: 4281904
    [No Abstract]   [Full Text] [Related]  

  • 10. A boy with trisomic Down's syndrome and a familial 5-?7 translocation, 47,XY,+21, t (5q-; ?7p+).
    Yanagisawa S
    Jinrui Idengaku Zasshi; 1972 Sep; 17(1):38-43. PubMed ID: 4265909
    [No Abstract]   [Full Text] [Related]  

  • 11. Familial C-G translocation causing mitotic nondisjunction. A cause of familial mosaic Down's syndrome.
    Weiss L; Wolf CB
    Am J Dis Child; 1968 Dec; 116(6):609-14. PubMed ID: 4235163
    [No Abstract]   [Full Text] [Related]  

  • 12. Down's syndrome at young maternal age; cytogenetical and genealogical study of eighty-two families.
    Mikkelson M
    Ann Hum Genet; 1967 Aug; 31(1):51-69. PubMed ID: 4228454
    [No Abstract]   [Full Text] [Related]  

  • 13. [Cytogenetic studies in children with Down's syndrome and in their relatives].
    Ostojska J
    Pediatr Pol; 1972 Oct; 47(10):1231-8. PubMed ID: 4263834
    [No Abstract]   [Full Text] [Related]  

  • 14. [Significance of chromosome translocations from the G-D group in the karyotype of the mother of 2 children with Down's syndrome].
    Dobrzańska A; Kostrzewski J
    Pediatr Pol; 1970 Feb; 45(2):211-5. PubMed ID: 4245096
    [No Abstract]   [Full Text] [Related]  

  • 15. [Familial pericentric inversion of y chromosome and Down's syndrome].
    García Sagredo JM; Morán Cabré A; San Román Cos-Gayón C
    An Esp Pediatr; 1975; 8(1):68-71. PubMed ID: 123717
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The importance of chromosome analysis in Down's syndrome. A case report of a 21-21 translocation.
    Eber LM; Goodman RM
    Ohio State Med J; 1966 Jan; 62(1):40-3. PubMed ID: 4232315
    [No Abstract]   [Full Text] [Related]  

  • 17. Patient with Down's syndrome and male pseudohermaphroditism with a 47, XY, plus21 karyotype.
    Mello RS; Souza OA; Santos Mello EM; Pimentel EC
    Clin Genet; 1974; 5(3):259-62. PubMed ID: 4275956
    [No Abstract]   [Full Text] [Related]  

  • 18. A familial tandem translocation (15;21) (q11;q22) in a case of Down's syndrome.
    Wahlström J; Djerg S
    J Ment Defic Res; 1976 Sep; 20(3):171-8. PubMed ID: 135089
    [No Abstract]   [Full Text] [Related]  

  • 19. [Report on a case of Down's syndrome with mosaicism. Trisomy 21-normal, clearly mongoloid phenotype and normal iliac index in a newborn infant].
    De Prà M; Lunetta Q
    Minerva Pediatr; 1974 Jan; 26(2):78-81. PubMed ID: 4276194
    [No Abstract]   [Full Text] [Related]  

  • 20. A rare translocation (47,XY,t(2p-;21q+),21+) associated with Down's syndrome.
    Miller JR; Dill FJ; Corey MJ; Rigg JM
    J Med Genet; 1970 Dec; 7(4):389-93. PubMed ID: 4250981
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.