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22. [Contribution to the clinical diagnosis of trisomy 21 on the basis of analysis of variance and discriminance]. Bach H, Bräunlich I, Freese E, Fröhlich M, Hauschild E, Hoffmeyer O, Jaeger U, Kunath H, Marischka E, Popella E, Seibt G, Sommer K, Thieme G. Z Arztl Fortbild (Jena); 1979 Jun 01; 73(11):520-5. PubMed ID: 157635 [No Abstract] [Full Text] [Related]
23. A survey of 972 cytogenetically examined cases of Down's syndrome. Gardner RJ, Veale AM, Parslow MI, Becroft DM, Shaw RL, Fitzgerald PH, Hutchings HE, McCreanor HR, Wong J, Eiby JR, Howarth DA, Whyte SE. N Z Med J; 1973 Nov 14; 78(502):403-9. PubMed ID: 4272131 [No Abstract] [Full Text] [Related]
24. Studying human chromosomes today. German J. Am Sci; 1970 Nov 14; 58(2):182-201. PubMed ID: 4244681 [No Abstract] [Full Text] [Related]
25. Structural aberrations of autosomes in a mentally retarded population. Corey MJ, Tischler B, Sandercock J. Am J Ment Defic; 1971 Jan 14; 75(4):487-98. PubMed ID: 4251270 [No Abstract] [Full Text] [Related]
26. Disease: its cause and effect. 2: Inherited and congenital disorders. Iveson-Iveson J. Nurs Mirror; 1979 Sep 20; 149(12):26-8. PubMed ID: 158180 [No Abstract] [Full Text] [Related]
27. [Clinically important chromosome aberrations]. Pelz L. Z Gesamte Inn Med; 1967 Mar 15; 22(6):Suppl:83-5. PubMed ID: 4232904 [No Abstract] [Full Text] [Related]
30. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)]. Butomo IV, Prozorova MV, Khitrikova LE. Tsitol Genet; 1984 Apr 15; 18(3):223-8. PubMed ID: 6235655 [Abstract] [Full Text] [Related]
31. [Significance of chromosomal mosaicism in clinical diagnosis and genetic counseling]. Vrba M, Brunecký Z. Cesk Pediatr; 1970 Sep 15; 25(9):435-8. PubMed ID: 4248283 [No Abstract] [Full Text] [Related]
32. [Down's syndrome with unusual karyotype: iso-pseudo-dicentric chromosome 21]. Kosztolányi G. Orv Hetil; 1988 Mar 06; 129(10):501-2. PubMed ID: 2966331 [No Abstract] [Full Text] [Related]
33. A case with 47,XXY,del(11)(q23) karotype-coexistence of Jacobsen and Klinefelter syndromes. Matheisel A, Babinska M, Wierzba J, Wozniak A, Nedoszytko B, Balcerska A, Limon J. Genet Couns; 2000 Mar 06; 11(3):267-71. PubMed ID: 11043435 [Abstract] [Full Text] [Related]
36. X-autosome translocation with a 47,XXXY qs,t(9p-;Xq+) karyotype. Dumars KW, Reed P, Lawce HJ. Birth Defects Orig Artic Ser; 1975 Mar 06; 11(5):247-53. PubMed ID: 1240775 [Abstract] [Full Text] [Related]
37. Probable reciprocal translocation in somatic cells from patients with Down's syndrome. Sonta S, Oishi H. Jinrui Idengaku Zasshi; 1974 Sep 06; 19(2):169-73. PubMed ID: 4280457 [No Abstract] [Full Text] [Related]
38. The utilization of fluorescent microscopy in routine chromosome analysis. Cullen SJ. J Am Med Womens Assoc (1972); 1973 Dec 06; 28(12):633-8. PubMed ID: 4358510 [No Abstract] [Full Text] [Related]
39. [Klinefelter's syndrome in children of mothers with sex chromosome anomalies]. Rosenkranz W. Helv Paediatr Acta; 1965 Sep 06; 20(4):359-68. PubMed ID: 5862851 [No Abstract] [Full Text] [Related]
40. Rates of chromosome abnormalities at different maternal ages. Hook EB. Obstet Gynecol; 1981 Sep 06; 58(3):282-5. PubMed ID: 6455611 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]