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 *

112 related articles for article (PubMed ID: 5488596)

  • 1. [Severe mesenchymosis in 2 infant brothers with congenital chromosome aberrations].
    Tarnoveanu G; Dobrescu G; Harmanschi A; Cighir R; Gheorghiu G; Anastasiu V; Mitescu G
    Presse Med (1893); 1970 Dec; 78(52):2322. PubMed ID: 5488596
    [No Abstract]   [Full Text] [Related]  

  • 2. [Chromosome aberrations and immunological deficiency].
    Calvani M
    Minerva Pediatr; 1977 Mar; 29(11):733-40. PubMed ID: 301598
    [No Abstract]   [Full Text] [Related]  

  • 3. Cytogenetic diseases.
    Nyhan WL
    Clin Symp; 1983; 35(1):1-32. PubMed ID: 6242703
    [No Abstract]   [Full Text] [Related]  

  • 4. [Nijmegen's syndrome].
    Kunz B; Teillac Hamel D; Girier B; Stephan JL; De Prost Y
    Ann Dermatol Venereol; 1992; 119(11):815-6. PubMed ID: 1301683
    [No Abstract]   [Full Text] [Related]  

  • 5. [Partial monosomy of the short arm of chromosome 10, associated with Rieger's syndrome and a Di George type partial immunodeficiency].
    Hervé J; Warnet JF; Jeaneau-Bellego E; Portnoi MF; Taillemitte JL; Hervé F
    Ann Pediatr (Paris); 1984 Jan; 31(1):77-80. PubMed ID: 6712103
    [No Abstract]   [Full Text] [Related]  

  • 6. "New" dwarfing syndromes.
    Spranger J
    Birth Defects Orig Artic Ser; 1977; 13(3B):11-29. PubMed ID: 407955
    [No Abstract]   [Full Text] [Related]  

  • 7. Cytogenetic study of Malaysian neonates with congenital abnormalities in Maternity Hospital Kuala Lumpur.
    Norlasiah IS; Clyde MM; Boo NY
    Med J Malaysia; 1995 Mar; 50(1):52-8. PubMed ID: 7752977
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Ineffective hemopoiesis, immunologic deficiency in two sisters with a missing C chromosome in bone marrow cell (author's transl)].
    Komiya M; Nomura T; Furusawa S; Adachi Y; Onozawa Y
    Nihon Ketsueki Gakkai Zasshi; 1973 Dec; 36(6):899-910. PubMed ID: 4800028
    [No Abstract]   [Full Text] [Related]  

  • 9. Partial trisomy 13 in an infant with a mild phenotype: application of fluorescence in situ hybridization in cytogenetic syndromes.
    Begovic D; Hitrec V; Lasan R; Letica L; Baric I; Sarnavka V; Galic S
    Croat Med J; 1998 Jun; 39(2):212-5. PubMed ID: 9575279
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Malformation syndromes caused by autosomal trisomies: Patau's syndrome and Edwards' syndrome].
    Rott HD; Schwanitz G; Meyer-Robisch M; Neubäuser G; Alexandrow G; Derbacher D; Ludwig H; Koch G
    Z Allgemeinmed; 1970 Dec; 46(34):1679-93. PubMed ID: 5518289
    [No Abstract]   [Full Text] [Related]  

  • 11. [Value of karyotyping in the diagnosis of collagenosis with respiratory involvement].
    Macquet V; Croquette MF; Rogeaux Y; Leduc M; Lafitte P
    LARC Med; 1984 Jan; 4(1):9-12. PubMed ID: 6717193
    [No Abstract]   [Full Text] [Related]  

  • 12. [Pätau syndrome with trisomy D 1 and D/D translocation].
    Tolksdorf M; Wiedemann HR; Hansen HG; Lehmann W
    Med Welt; 1965 Oct; 41():2304-7. PubMed ID: 5864766
    [No Abstract]   [Full Text] [Related]  

  • 13. [A recent case of trisomy 13].
    Gaudier B; Ponté C; Walbaum R; Leduc M; Desbonnets P; Ryckewaert P; Delattre B
    Pediatrie; 1968 Mar; 23(2):215-26. PubMed ID: 5739918
    [No Abstract]   [Full Text] [Related]  

  • 14. Developmental and other pathologic changes in syndromes caused by chromosome abnormalities.
    Gilbert EF; Opitz JM
    Perspect Pediatr Pathol; 1982; 7():1-63. PubMed ID: 6214761
    [No Abstract]   [Full Text] [Related]  

  • 15. An infant with double trisomy (48,XXX, + 18).
    Jaruratanasirikul S; Jinorose U
    Am J Med Genet; 1994 Jan; 49(2):207-10. PubMed ID: 8116670
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Trisomy 13 syndrome (Patau syndrome), trisomy 18 syndrome (Edwards syndrome), Down syndrome (trisomy 21 syndrome), Turner syndrome (XO gonadal dysgenesis)].
    Harada N; Niikawa N
    Ryoikibetsu Shokogun Shirizu; 1996; (15):198-201. PubMed ID: 9047985
    [No Abstract]   [Full Text] [Related]  

  • 17. Double trisomy (48,XXX, +18).
    Tsukahara M; Fukuda M; Furukawa S; Kondoh O
    Am J Med Genet; 1994 Aug; 52(2):244. PubMed ID: 7802021
    [No Abstract]   [Full Text] [Related]  

  • 18. [Chromosome aberrations in fetuses and neonates].
    Boczkowski K
    Postepy Hig Med Dosw; 1981; 34(6):479-89. PubMed ID: 7291083
    [No Abstract]   [Full Text] [Related]  

  • 19. [Trisomy syndrome D (47, XY, D+) in a newborn].
    Majlert T; Jaworska M; Stolarska A
    Pediatr Pol; 1970 Nov; 45(11):1379-82. PubMed ID: 5496174
    [No Abstract]   [Full Text] [Related]  

  • 20. [On grave mesenchymopathies in infants. Description of a new clinical form: myoarthropathic mesenchymopathy with endomyocardial sclerohyalinosis, immune deficit and congenital chromosome aberrations].
    Tîrnoveanu G; Dobrescu G; Harmanschi A; Cighir R; Gheorghiu C; Anastasiu V; Mitescu G
    Pediatria (Bucur); 1971; 20(6):505-15. PubMed ID: 4112141
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.