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.
35. Comparative study of sole patterns in chromosomal abnormalities. Penrose LS, Loesch D. J Ment Defic Res; 1970 Jun 22; 14(2):129-40. PubMed ID: 5512213 [No Abstract] [Full Text] [Related]
36. [Pathology of constitutional autosomal anomalies]. Constantinescu C, Diculescu G. Pediatria (Bucur); 1966 Jun 22; 15(6):497-512. PubMed ID: 4226965 [No Abstract] [Full Text] [Related]
37. [Ocular findings in chromosome diseases]. Cagianut B. Ophthalmologica; 1968 Jun 22; 155(2):148-66. PubMed ID: 4965902 [No Abstract] [Full Text] [Related]
38. [Clinical chromosome anomalies (1st part) (author's transl)]. Klein D. Schweiz Rundsch Med Prax; 1975 Feb 11; 64(6):148-60. PubMed ID: 129770 [No Abstract] [Full Text] [Related]
39. [46,XX,r(18), + mar karyotype in the niece of a leukemic patient with trisomy 21 and cri du chat chromosome (author's transl)]. Koulischer L, Gillerot Y, Richard J. Ann Genet; 1980 Feb 11; 23(4):228-31. PubMed ID: 6452850 [Abstract] [Full Text] [Related]
40. [The clinical manifestations and cytogenetic observations of 7 cases affected by the cri-du-chat syndrome]. Mennicken U, Pfeiffer RA, Puyn U, Worbes H, Wagener A. Z Kinderheilkd; 1968 Oct 09; 104(3):230-56. PubMed ID: 5724306 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]