214 related articles for article (PubMed ID: 6938131)
1. Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome).
Jennings M; Hall JG; Hoehn H
Am J Med Genet; 1980; 7(4):417-32. PubMed ID: 6938131
[TBL] [Abstract][Full Text] [Related]
2. X-linked mental retardation with macro-orchidism and marker-X chromosomes.
Martin RH; Lin CC; Mathies BJ; Lowry RB
Am J Med Genet; 1980; 7(4):433-41. PubMed ID: 6938132
[TBL] [Abstract][Full Text] [Related]
3. Nonspecific X-linked mental retardation I: a review with information from 24 new families.
Herbst DS
Am J Med Genet; 1980; 7(4):443-60. PubMed ID: 7011032
[TBL] [Abstract][Full Text] [Related]
4. X-linked mental retardation: a study of 7 families.
Jacobs PA; Glover TW; Mayer M; Fox P; Gerrard JW; Dunn HG; Herbst DS
Am J Med Genet; 1980; 7(4):471-89. PubMed ID: 7211957
[TBL] [Abstract][Full Text] [Related]
5. [X chromosome-linked mental retardation with fragile X chromosome and macro-orchidism].
Zollinger A; Schmid W; Vilan J; Sorg B; Knoblauch M
Schweiz Med Wochenschr; 1983 Feb; 113(7):238-44. PubMed ID: 6836249
[TBL] [Abstract][Full Text] [Related]
6. X-linked mental retardation. I. Martin-Bell syndrome (report of 18 families).
Rocchi M; Archidiacono N; Filippi G
J Genet Hum; 1987 Dec; 35(5):351-79. PubMed ID: 3437265
[TBL] [Abstract][Full Text] [Related]
7. The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers.
Fishburn J; Turner G; Daniel A; Brookwell R
Am J Med Genet; 1983 Apr; 14(4):713-24. PubMed ID: 6682625
[TBL] [Abstract][Full Text] [Related]
8. X-linked mental retardation. II. Renpenning syndrome and other types (report of 14 families).
Archidiacono N; Rocchi M; Rinaldi A; Filippi G
J Genet Hum; 1987 Dec; 35(5):381-98. PubMed ID: 3437266
[TBL] [Abstract][Full Text] [Related]
9. Fragile X chromosome and X-linked mental retardation.
Larbrisseau A; Jean P; Messier B; Richer CL
Can Med Assoc J; 1982 Jul; 127(2):123-6. PubMed ID: 7093857
[TBL] [Abstract][Full Text] [Related]
10. Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).
Turner G; Brookwell R; Daniel A; Selikowitz M; Zilibowitz M
N Engl J Med; 1980 Sep; 303(12):662-4. PubMed ID: 6931286
[TBL] [Abstract][Full Text] [Related]
11. [Fragile X chromosome and X-linked mental retardation (author's transl)].
Fonatsch C; Flatz SD
Wien Klin Wochenschr; 1982 Apr; 94(8):217-9. PubMed ID: 7101956
[TBL] [Abstract][Full Text] [Related]
12. Fragile X-linked mental retardation. A survey of 65 patients with mental retardation of unknown origin.
Carpenter NJ; Leichtman LG; Say B
Am J Dis Child; 1982 May; 136(5):392-8. PubMed ID: 7081157
[TBL] [Abstract][Full Text] [Related]
13. X-linked mental retardation.
Turner G; Opitz JM
Am J Med Genet; 1980; 7(4):407-15. PubMed ID: 7011031
[No Abstract] [Full Text] [Related]
14. Fragile sites in human chromosomes II: demonstration of the fragile site Xq27 in carriers of X-linked mental retardation.
Howard-Peebles PN
Am J Med Genet; 1980; 7(4):497-501. PubMed ID: 6938133
[TBL] [Abstract][Full Text] [Related]
15. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3.
Goonewardena P; Dahl N; Gustavson KH; Holmgren G; Pettersson U
Ups J Med Sci Suppl; 1987; 44():155-64. PubMed ID: 2895524
[TBL] [Abstract][Full Text] [Related]
16. Mental retardation, megalotestes and a marker X chromosome.
Fitzsimmons J; McLachlan JI; Fitzsimmons E; Cooke P
Practitioner; 1982 Apr; 226(1366):735-41. PubMed ID: 6953399
[No Abstract] [Full Text] [Related]
17. Familial X-linked mental retardation syndrome associated with minor congenital anomalies, macro-orchidism, and fragile X-chromosome.
Pueschel SM; Hays RM; Mendoza T
Am J Ment Defic; 1983 Jan; 87(4):372-6. PubMed ID: 6829615
[TBL] [Abstract][Full Text] [Related]
18. [X-linked mental retardation, macro-orchism, and X chromosome fragile site. Presentation of 6 cases in 2 families].
Pascual-Castroviejo I; López Pajares I; Delicado A
An Esp Pediatr; 1982 Dec; 17(6):466-74. PubMed ID: 6892145
[TBL] [Abstract][Full Text] [Related]
19. The fragile X syndrome (Martin-Bell syndrome). Clinical and cytogenetic findings in 16 prepubertal boys and in 4 of their 5 families.
Schinzel A; Largo RH
Helv Paediatr Acta; 1985 Jul; 40(2-3):133-52. PubMed ID: 3843245
[TBL] [Abstract][Full Text] [Related]
20. Marker X syndrome in an oriental family with probable transmission by a normal male.
Rhoads FA; Oglesby AC; Mayer M; Jacobs PA
Am J Med Genet; 1982 Jun; 12(2):205-17. PubMed ID: 7102725
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
