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 *

126 related articles for article (PubMed ID: 4122450)

  • 1. Points of exchange in a human no. 5 ring chromosome.
    Nakagome Y; Iinume K; Taniguchi K
    Cytogenet Cell Genet; 1973; 12(1):35-9. PubMed ID: 4122450
    [No Abstract]   [Full Text] [Related]  

  • 2. Transmission of the cri-du-chat syndrome from a maternal balanced translocation carrier, t(5p-;11q+).
    Singh DN; Osborne RA; Wiscovitch RA
    Humangenetik; 1973 Dec; 20(4):361-5. PubMed ID: 4768112
    [No Abstract]   [Full Text] [Related]  

  • 3. Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the "cri du chat" syndrome.
    Faed MJ; Marrian VJ; Robertson J; Robson EB; Cook PJ
    Cytogenetics; 1972; 11(5):400-11. PubMed ID: 4119109
    [No Abstract]   [Full Text] [Related]  

  • 4. A 45,XY,5-15-,t(5q15q) cri-du-chat child.
    Jackson L; Barr M
    J Med Genet; 1970 Jun; 7(2):161-3. PubMed ID: 5519604
    [No Abstract]   [Full Text] [Related]  

  • 5. "Cri du chat" syndrome with maternal insertional translocation.
    Berger R; Touati G; Derre J; Ortiz MA; Martinetti J
    Clin Genet; 1974; 5(5):428-32. PubMed ID: 4368036
    [No Abstract]   [Full Text] [Related]  

  • 6. Ring chromosome 5 in two malformed boys with Cri du Chat syndrome.
    Suerinck E; Noël B; Rethore MO
    Clin Genet; 1978 Sep; 14(3):125-9. PubMed ID: 699350
    [No Abstract]   [Full Text] [Related]  

  • 7. New techniques in the study of human chromosomes: methods and applications.
    Dutrillaux B; Lejeune J
    Adv Hum Genet; 1975; 5():119-56. PubMed ID: 48327
    [No Abstract]   [Full Text] [Related]  

  • 8. Cri du chat syndrome [46, XY, 5p-] with balanced B/F translocation in father and grandfather: a case report.
    Char F
    Birth Defects Orig Artic Ser; 1974; 10(10):49-53. PubMed ID: 4462641
    [No Abstract]   [Full Text] [Related]  

  • 9. A 45,XX,5-,13-,dic+ karyotype in a case of cri-du-chat syndrome.
    Niebuhr E
    Cytogenetics; 1972; 11(3):165-77. PubMed ID: 5038360
    [No Abstract]   [Full Text] [Related]  

  • 10. Cytologic observations in 35 individuals with a 5p- karyotype.
    Niebuhr E
    Hum Genet; 1978 Jun; 42(2):143-56. PubMed ID: 669700
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Deficiency of the short arm of chromosome. 5. Crying cat syndrome].
    Berger R
    Nouv Presse Med; 1972 Mar; 1(13):873-5. PubMed ID: 5018461
    [No Abstract]   [Full Text] [Related]  

  • 12. [Crying cat disease associated with complex chromosome rearrangement in a dizygotic twin].
    Taillemite JL; Baheux-Morlier G; Cathelineau L; Roux C
    Ann Genet; 1973 Jun; 16(2):127-30. PubMed ID: 4541905
    [No Abstract]   [Full Text] [Related]  

  • 13. The "cri du chat" syndrome.
    Mladkovskaya TB; Lebedev BV; Mazaeva IV
    Sov Genet; 1970 Oct; 6(10):1374-9. PubMed ID: 4272596
    [No Abstract]   [Full Text] [Related]  

  • 14. De novo appearance of a translocation t(5p; 2Iq), and its transmission in both balanced and unbalanced forms to the next generation.
    Chaganti RS; Morillo-Cucci G; Friis L; Degnan M; German J
    Ann Genet; 1976 Mar; 19(1):43-8. PubMed ID: 1084121
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Possible localisation of the gene for cystic fibrosis of the pancreas to the short arm of chromosome 5.
    Smith DW; Docter JM; Ferrier PE; Frias JL; Spock A
    Lancet; 1968 Aug; 2(7563):309-12. PubMed ID: 4173733
    [No Abstract]   [Full Text] [Related]  

  • 16. Cri-du-chat syndrome in a child with a 5/15 translocation and interstitial centromeric heterochromatin.
    Gebauer HJ; Stumpf B; Hansmann I; Grimm T
    Clin Genet; 1978 Dec; 14(6):345-50. PubMed ID: 83210
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. Mosaic Cri du Chat syndrome in a patient exhibiting three 5p cell lines.
    Kitsiou S; Kolialexi A; Mavrou A
    Prenat Diagn; 2004 Jul; 24(7):578-9. PubMed ID: 15300755
    [No Abstract]   [Full Text] [Related]  

  • 19. Deletion of the short arm of chromosome 5 from a subject with cri-du-chat syndrome respository identification no. GM-71.
    Breg WR; Aronson MM; Greene AE; Coriell LL
    Cytogenet Cell Genet; 1976; 17(4):239-40. PubMed ID: 1001031
    [No Abstract]   [Full Text] [Related]  

  • 20. Identification of the abnormal B group chromosome in the "cri du chat" syndrome by QM-fluorescence.
    Caspersson T; Lindsten J; Zech L
    Exp Cell Res; 1970 Aug; 61(2):475-6. PubMed ID: 5459851
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.