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5. Pure gonadal dysgenesis; clinical and genetic studies. Boczkowski K Mater Med Pol; 1973; 5(3):197-202. PubMed ID: 4749978 [No Abstract] [Full Text] [Related]
6. [CHROMOSOME ABERRATIONS]. GILGENKRANTZ S; OLIVE D; PIERSON M Ann Med Nancy; 1963; 2():1029-60. PubMed ID: 14078788 [No Abstract] [Full Text] [Related]
8. Turner's syndrome: cytogenetic study of a patient included in the initial report of Turner. Sparkes RS; Kolodny S J Clin Endocrinol Metab; 1966 May; 26(5):577-9. PubMed ID: 5938373 [No Abstract] [Full Text] [Related]
9. [Dermatoglyphics in normal and pathological conditions. Review of current knowledge]. Ceccarelli M; Giorgi PL; Paci A Minerva Pediatr; 1967 Dec; 19(50):2229-36. PubMed ID: 4237109 [No Abstract] [Full Text] [Related]
16. [Dermatoglyphics in the syndromes caused by sex chromosome aberrations]. Dallapiccola B Folia Endocrinol; 1966 Jun; 19(3):355-67. PubMed ID: 6012944 [No Abstract] [Full Text] [Related]
17. XX and XY Turner phenotypes in a family. Levy EP; Pashayan H; Fraser FC; Pinsky L Am J Dis Child; 1970 Jul; 120(1):36-43. PubMed ID: 5422855 [No Abstract] [Full Text] [Related]
18. FAMILIAL MOSAICISM OF A CHROMOSOME 16 ABNORMALITY ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES. TIPS RL; SMITH GS; MEYER DL; PERKINS AL Am J Ment Defic; 1964 Nov; 69():330-40. PubMed ID: 14223550 [No Abstract] [Full Text] [Related]
19. Familial occurrence of Noonan syndrome. Qazi QH; Arnon RG; Paydar MH; Mapa HC Am J Dis Child; 1974 May; 127(5):696-8. PubMed ID: 4151095 [No Abstract] [Full Text] [Related]