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.
191 related articles for article (PubMed ID: 4550373)
21. Two human X-autosome translocations identified by autoradiography and fluorescence. Cohen MM; Lin CC; Sybert V; Orecchio EJ Am J Hum Genet; 1972 Sep; 24(5):583-97. PubMed ID: 5054227 [No Abstract] [Full Text] [Related]
22. Cytogenetics in medical practice. Nelson MM; Beighton PH S Afr Med J; 1974 Aug; 48(37):1577-80. PubMed ID: 4277424 [No Abstract] [Full Text] [Related]
23. A case of quintuple-X syndrome (49,XXXXX). Zajaczkowska K; Korniszewski L; Wolff-Plodowska A J Ment Defic Res; 1970 Dec; 14(4):305-11. PubMed ID: 5517968 [No Abstract] [Full Text] [Related]
24. Sex chromatin survey among mentally retarded children in Japan. Yanagisawa S; Shuto T J Ment Defic Res; 1970 Sep; 14(3):254-62. PubMed ID: 5518410 [No Abstract] [Full Text] [Related]
25. [Clinical and cytogenetic findings in a rare autosomal aberrations]. Tolksdorf M Monatsschr Kinderheilkd (1902); 1970 Jun; 118(6):308-13. PubMed ID: 5523669 [No Abstract] [Full Text] [Related]
26. A case of 48,XXXX female with normal intelligence. Blackston RD; Chen AT J Med Genet; 1972 Jun; 9(2):230-2. PubMed ID: 5046634 [No Abstract] [Full Text] [Related]
27. Conenital hypothyroidism in association with a ring chromosome 18. Winter JS; Ahluwalia K; Ray M J Med Genet; 1972 Mar; 9(1):122-6. PubMed ID: 5025476 [No Abstract] [Full Text] [Related]
28. [Sex chromatin test in the diagnosis of cases of primary amenorrhea]. Binkiewicz B; Boczkowski K Ginekol Pol; 1967; 38(10):1149-52. PubMed ID: 6064112 [No Abstract] [Full Text] [Related]
29. Human cytogenetics: 46 chromosomes, 46 years and counting. Trask BJ Nat Rev Genet; 2002 Oct; 3(10):769-78. PubMed ID: 12360235 [TBL] [Abstract][Full Text] [Related]
30. An XXsex chromosome complement in an infant having male-type external genitals, renal agenesis, and other anomalies. Schlegel RJ; Aspillaga MJ; Neu RL; Carneiro-Leão J; Gardner LI J Pediatr; 1966 Nov; 69(5):812-3. PubMed ID: 5928014 [No Abstract] [Full Text] [Related]
31. Sex chromatin frequency in buccal mucosal tissue: the distribution of single, double and triple sex chromatin bodies. Curtis DJ Humangenetik; 1970; 11(1):22-8. PubMed ID: 5490352 [No Abstract] [Full Text] [Related]
32. Human chromosome abnormalities as related to physical and mental dysfunction. Heller JH J Hered; 1969; 60(5):239-48. PubMed ID: 4244249 [No Abstract] [Full Text] [Related]
33. Multiple anomalies associated with a small extra metacentric autosome. Mukherjee AB; Partington MW; Simpson NE; Walmsley KA J Med Genet; 1968 Dec; 5(4):329-34. PubMed ID: 5713649 [No Abstract] [Full Text] [Related]
34. [Chromosomal mosaicism in humans]. Covic M; Angheloni T Rev Med Chir Soc Med Nat Iasi; 1972; 76(2):385-94. PubMed ID: 4507493 [No Abstract] [Full Text] [Related]
35. [Trisomy of group C (47, XX, C+)]. Emberger JM; Rey J; Rieu D; Dossa D; Bonnet H; Jean R Arch Fr Pediatr; 1970; 27(10):1081-8. PubMed ID: 5495708 [No Abstract] [Full Text] [Related]
36. The infant with ambiguous genitalia. Moloshok RE; Kerr JM Pediatr Clin North Am; 1972 Aug; 19(3):529-42. PubMed ID: 5039348 [No Abstract] [Full Text] [Related]
37. A patient with 45,X-46,XXq--46,XXq-dic karyotype. Stevenson AC; Bedford J; Barberton GM J Med Genet; 1971 Dec; 8(4):513-6. PubMed ID: 5149536 [No Abstract] [Full Text] [Related]
38. RECENT ADVANCES IN HUMAN CYTOGENETICS. SMITH KD; STEINBERGER E; STEINBERGER A; PERLOFF WH J Albert Einstein Med Cent (Phila); 1963 Jul; 11():134-58. PubMed ID: 14044060 [No Abstract] [Full Text] [Related]