163 related articles for article (PubMed ID: 8330452)
21. [49,XXXXY syndrome in a 5-year-old boy].
Wiśniewski L; Krajewska-Walasek M; Lech H; Mospinek M
Pediatr Pol; 1980 Jan; 55(1):81-6. PubMed ID: 7189276
[No Abstract] [Full Text] [Related]
22. Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.
Ballabio A; Bardoni B; Carrozzo R; Andria G; Bick D; Campbell L; Hamel B; Ferguson-Smith MA; Gimelli G; Fraccaro M
Proc Natl Acad Sci U S A; 1989 Dec; 86(24):10001-5. PubMed ID: 2602357
[TBL] [Abstract][Full Text] [Related]
23. Female phenotype and multiple abnormalities in sibs with a Y chromosome and partial X chromosome duplication: H--Y antigen and Xg blood group findings.
Bernstein R; Jenkins T; Dawson B; Wagner J; Dewald G; Koo GC; Wachtel SS
J Med Genet; 1980 Aug; 17(4):291-300. PubMed ID: 7193738
[TBL] [Abstract][Full Text] [Related]
24. Neuropsychiatric disturbances in a patient with a nonmosaic isodicentric (X) (q21.32) chromosome.
Suzuki T; Koizumi J; Arinami T; Shiraishi H; Ofuku K; Kawai N; Baba A; Ninomiya H
Jpn J Psychiatry Neurol; 1990 Sep; 44(3):563-70. PubMed ID: 2127433
[TBL] [Abstract][Full Text] [Related]
25. Interstitial deletion of the long arm of chromosome 6.
Chery M; Formiga LF; Mujica P; André M; Stehelin D; Dozier C; Gilgenkrantz S
Ann Genet; 1989; 32(2):82-6. PubMed ID: 2757364
[TBL] [Abstract][Full Text] [Related]
26. [48,XXYY syndrome in a boy with essential tremor. Comparison with 120 cases from the literature].
Donati F; Gasser S; Mullis P; Braga S; Vassella F
Monatsschr Kinderheilkd; 1992 Apr; 140(4):216-9. PubMed ID: 1614446
[TBL] [Abstract][Full Text] [Related]
27. [Fraccaro's syndrome: 49XXXXY sexual polysomy. Apropos of 2 cases].
Fontoura M; López-Herce Cid J; Rodríguez Sánchez C; Duelo M; González M; Gracia R; Oliver A; Peralta A
An Esp Pediatr; 1986 Jan; 24(1):71-3. PubMed ID: 3963649
[No Abstract] [Full Text] [Related]
28. [Radioulnar synostosis as characteristic feature of chromosome aberrations (author's transl)].
Küsswetter W; Heisel A
Z Orthop Ihre Grenzgeb; 1981 Feb; 119(1):10-3. PubMed ID: 7281903
[TBL] [Abstract][Full Text] [Related]
29. X linked mental retardation with non-deletional alpha thalassaemia (ATR-X): further delineation of the phenotype.
Ogle R; DeSouza M; Cunningham C; Kerr B; Sillence D
J Med Genet; 1994 Mar; 31(3):245-7. PubMed ID: 8014976
[TBL] [Abstract][Full Text] [Related]
30. Coffin-Lowry syndrome: a multicenter study.
Gilgenkrantz S; Mujica P; Gruet P; Tridon P; Schweitzer F; Nivelon-Chevallier A; Nivelon JL; Couillault G; David A; Verloes A
Clin Genet; 1988 Oct; 34(4):230-45. PubMed ID: 3069251
[TBL] [Abstract][Full Text] [Related]
31. [Recent advances in the genetics and physiopathology of X chromosomal mental retardation].
Chelly J
Arch Pediatr; 2000 May; 7 Suppl 2():114s-118s. PubMed ID: 10904677
[No Abstract] [Full Text] [Related]
32. Characterisation of an inverted X chromosome (p11.2q21.3) associated with mental retardation using FISH.
Sloan-Béna F; Philippe C; LeHeup B; Wuilque F; Levy ER; Chéry M; Jonveaux P; Monaco AP
J Med Genet; 1998 Feb; 35(2):146-50. PubMed ID: 9507395
[TBL] [Abstract][Full Text] [Related]
33. Marker (X)-linked mental retardation.
Turner G; Jacobs P
Adv Hum Genet; 1983; 13():83-112. PubMed ID: 6362362
[No Abstract] [Full Text] [Related]
34. Pentasomy X: report of patient and studies of X-inactivation.
Funderburk SJ; Valente M; Klisak I
Am J Med Genet; 1981; 8(1):27-33. PubMed ID: 7246603
[TBL] [Abstract][Full Text] [Related]
35. Identification and characterisation of a small marker chromosome using non-isotopic in situ hybridisation with X and Y specific probes.
Crolla JA; Smith M; Docherty Z
J Med Genet; 1989 Mar; 26(3):192-4. PubMed ID: 2709396
[TBL] [Abstract][Full Text] [Related]
36. Microcephaly, mental retardation and hypertelorism in chromosome deletion studies.
Miller JQ
Neurology; 1973 Nov; 23(11):1141-6. PubMed ID: 4795737
[No Abstract] [Full Text] [Related]
37. [Mental retardation linked to the X chromosome].
Lambotte C
Rev Med Liege; 1982 Feb; 37(4):130-9. PubMed ID: 7079652
[No Abstract] [Full Text] [Related]
38. Ring chromosome 6: case report and review of literature.
Kini KR; Van Dyke DL; Weiss L; Logan MS
Hum Genet; 1979; 50(2):145-9. PubMed ID: 511129
[TBL] [Abstract][Full Text] [Related]
39. X-linked mental retardation with the fragile X. A study of 15 families.
Mattei JF; Mattei MG; Aumeras C; Auger M; Giraud F
Hum Genet; 1981; 59(4):281-9. PubMed ID: 7333582
[TBL] [Abstract][Full Text] [Related]
40. Severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphism.
Devriendt K; Keymolen K; Roelen L; Van Goethem G; Meireleire J; Fryns JP
Clin Dysmorphol; 2000 Apr; 9(2):111-4. PubMed ID: 10826622
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]