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Journal Abstract Search
179 related items for PubMed ID: 3591842
1. Fragile X transmission and the determination of carrier probabilities for genetic counseling. Mulley JC, Sutherland GR. Am J Med Genet; 1987 Apr; 26(4):987-90. PubMed ID: 3591842 [No Abstract] [Full Text] [Related]
2. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14. Mulley JC, Gedeon AK, Thorn KA, Bates LJ, Sutherland GR. Am J Med Genet; 1987 Jun; 27(2):435-48. PubMed ID: 2886048 [Abstract] [Full Text] [Related]
6. [Fragile X syndrome: what do we know today?]. Ramos FJ. An Esp Pediatr; 1989 Nov; 31(5):417-9. PubMed ID: 2575879 [No Abstract] [Full Text] [Related]
7. Fragile X syndrome associated with Tourette symptomatology in a male with moderate mental retardation and autism. Kerbeshian J, Burd L, Martsolf JT. J Dev Behav Pediatr; 1984 Aug; 5(4):201-3. PubMed ID: 6590572 [No Abstract] [Full Text] [Related]
9. The fragile X syndrome. Brown WT. Neurol Clin; 1989 Feb; 7(1):107-21. PubMed ID: 2646518 [Abstract] [Full Text] [Related]
10. [(Fra)X in male cousins with mental retardation]. Rozynkowa D, Górski G, Jabłońska R. Pediatr Pol; 1986 Jul; 61(7):441-5. PubMed ID: 3822610 [No Abstract] [Full Text] [Related]
11. Cytogenetic survey for autistic fragile X carriers in a mental retardation center. Cantú ES, Stone JW, Wing AA, Langee HR, Williams CA. Am J Ment Retard; 1990 Jan; 94(4):442-7. PubMed ID: 2297426 [Abstract] [Full Text] [Related]
13. A counseling guide to the Martin-Bell syndrome. Weaver DD, Sherman SL. Am J Med Genet; 1987 Jan; 26(1):39-44. PubMed ID: 3812576 [No Abstract] [Full Text] [Related]