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 *

121 related articles for article (PubMed ID: 4641844)

  • 1. A case of the 18p--syndrome.
    Subrt I; Beránková J
    Humangenetik; 1972; 16(4):359-60. PubMed ID: 4641844
    [No Abstract]   [Full Text] [Related]  

  • 2. [E 18 ring chromosome--case report and review].
    Grosse KP; Schwanitz G; Rott HD; Klein K; von Zyl J
    Klin Padiatr; 1972 Nov; 184(6):495-500. PubMed ID: 4675258
    [No Abstract]   [Full Text] [Related]  

  • 3. [The clinical features of the 18 q-syndrome (author's transl)].
    Feichtinger C; Glatzl J
    Wien Klin Wochenschr; 1974 Aug; 86(15):441-4. PubMed ID: 4605988
    [No Abstract]   [Full Text] [Related]  

  • 4. [Morphologic abnormality due to duplication of chromosome 17 (46,XY,17q+) in a newborn infant].
    Fouquette B; Rosenfeld R; Cadotte M
    Union Med Can; 1974 Aug; 103(8):1404-8. PubMed ID: 4849205
    [No Abstract]   [Full Text] [Related]  

  • 5. A short, retarded child with a deletion of the short arm of chromosome 18 (18p-).
    Parker CE; Donnell GN; Mavalwala J; Hurst N; Derencsenyi A
    Clin Pediatr (Phila); 1973 Jan; 12(1):42-6. PubMed ID: 4345621
    [No Abstract]   [Full Text] [Related]  

  • 6. [Ring chromosome 18. 18p-/18q- -deletion-syndrome].
    Kunze J; Stephan E; Tolksdorf M
    Humangenetik; 1972; 15(4):289-318. PubMed ID: 4565746
    [No Abstract]   [Full Text] [Related]  

  • 7. Trisomy-18 mosaicism with features of Russel-Silver syndrome.
    Chauvel PJ; Moore CM; Haslam RH
    Dev Med Child Neurol; 1975 Apr; 17(2):220-4. PubMed ID: 1132609
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Malformation syndrome in autosomal deficiency (D2-G1)].
    Pfeiffer RA; Bachmann KD; Bartel K
    Z Kinderheilkd; 1967; 100(4):279-90. PubMed ID: 5596635
    [No Abstract]   [Full Text] [Related]  

  • 9. De novo deletion of chromosome 9 (9p-) in a child with multiple congenital anomalies and psychomotor retardation.
    Murthy DS; Murthy SK; Banker GJ; Patel AJ
    Indian Pediatr; 1991 May; 28(5):546-9. PubMed ID: 1684352
    [No Abstract]   [Full Text] [Related]  

  • 10. Ring chromosome 15 syndrome.
    Fryns JP; Jaeken J; Devlieger H; Debucquoy P; Eggermont E; Van den Berghe H
    Acta Paediatr Belg; 1981; 34(1):47-9. PubMed ID: 7270144
    [No Abstract]   [Full Text] [Related]  

  • 11. Prenatal chromosome determination. A study of 219 cases.
    Wahlström J; Bartsch FK; Lundberg J
    Clin Genet; 1974; 6(3):184-91. PubMed ID: 4279153
    [No Abstract]   [Full Text] [Related]  

  • 12. Edwards' syndrome with double trisomy (possible tetrasomy) of the E group chromosomes (17-18).
    Korányi G; László J
    Acta Paediatr Acad Sci Hung; 1969; 10(2):167-75. PubMed ID: 5367786
    [No Abstract]   [Full Text] [Related]  

  • 13. [The deletion of the short arm of chromosome 18 (18p- syndrome), apropos of a new observation].
    Gilgenkrantz S; Marchal C; Neimann N
    Ann Genet; 1968 Mar; 11(1):17-21. PubMed ID: 5301751
    [No Abstract]   [Full Text] [Related]  

  • 14. [Tendency for chromosome breaks in Russel's syndrome].
    Ganner E; Schwingshackl A
    Klin Wochenschr; 1970 May; 48(10):629-32. PubMed ID: 5517331
    [No Abstract]   [Full Text] [Related]  

  • 15. The clinical and genetic picture of trisomy 18 (Edwards' syndrome).
    Shibata K; Waldenmaier C; Hirsch W
    Z Kinderheilkd; 1973 Dec; 116(1):13-22. PubMed ID: 4129502
    [No Abstract]   [Full Text] [Related]  

  • 16. [Eye anomalies in chromosomal aberrations].
    Lur'e IV; Gushchina GS
    Oftalmol Zh; 1971; 26(4):299-306. PubMed ID: 4256612
    [No Abstract]   [Full Text] [Related]  

  • 17. [Syndrome of ring deletion of group E chromosome in a female infant].
    Baniowski A; Kleczkowska A; Kubień E; Sokolowski J
    Pediatr Pol; 1971 Sep; 46(9):1167-70. PubMed ID: 5114250
    [No Abstract]   [Full Text] [Related]  

  • 18. [Ocular findings in chromosome diseases].
    Cagianut B
    Ophthalmologica; 1968; 155(2):148-66. PubMed ID: 4965902
    [No Abstract]   [Full Text] [Related]  

  • 19. Identification of 21r and 22r chromosomes by quinacrine fluorescence.
    Crandall BF; Weber F; Muller HM; Burwell JK
    Clin Genet; 1972; 3(4):264-70. PubMed ID: 5054320
    [No Abstract]   [Full Text] [Related]  

  • 20. [Ocular manifestations of trisomy 18].
    Ardouin M; Urvoy M; Lautridou A; Le Marec B; Senecal J
    Arch Ophtalmol Rev Gen Ophtalmol; 1972; 32(6):457-76. PubMed ID: 4264548
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.