191 related articles for article (PubMed ID: 568665)
1. Chromosome banding studies in two patients with XXXXY syndrome.
Levy CL; Sparkes RS; Carlson HE
J Med Genet; 1978 Aug; 15(4):301-5. PubMed ID: 568665
[TBL] [Abstract][Full Text] [Related]
2. Epiphysial dysplasia: a constant finding in the XXXXY syndrome.
Schmidt R; Pajewski M; Rosenblatt M
J Med Genet; 1978 Aug; 15(4):282-7. PubMed ID: 568664
[TBL] [Abstract][Full Text] [Related]
3. Cytogenetic studies in a selected group of mentally retarded children.
Moghe M; Patel ZM; Peter JJ; Ambani LM
Hum Genet; 1981; 58(2):184-7. PubMed ID: 6456981
[TBL] [Abstract][Full Text] [Related]
4. 49, XXXXY karyotype in mentally retarded boy.
Morić-Petrović S; Laca Z; Marković S; Marković V
J Ment Defic Res; 1973 Mar; 17(1):73-80. PubMed ID: 4795155
[No Abstract] [Full Text] [Related]
5. Screening for fra(X)(q) in a population of mentally retarded males.
Froster-Iskenius U; Felsch G; Schirren C; Schwinger E
Hum Genet; 1983; 63(2):153-7. PubMed ID: 6682403
[TBL] [Abstract][Full Text] [Related]
6. Mild intellectual deficits in a child with 49,XXXXY.
Hersh JH; Bloom AS; Yen F; Topinka C; Weisskopf B
Res Dev Disabil; 1988; 9(2):171-6. PubMed ID: 3406471
[TBL] [Abstract][Full Text] [Related]
7. 49,XXXXX syndrome.
Fragoso R; Hernandez A; Plascencia ML; Nazara Z; Martinez y Martinez R; Cantu JM
Ann Genet; 1982; 25(3):145-8. PubMed ID: 6982661
[TBL] [Abstract][Full Text] [Related]
8. Sex chromosome pentasomy 49,XXXXY connected with hypothyroidism. Case report.
Wikiera B; Głab E; Slezak R; Wójcik E; Noczyńska A
Pediatr Endocrinol Diabetes Metab; 2009; 15(2):125-7. PubMed ID: 19772821
[TBL] [Abstract][Full Text] [Related]
9. The 49,XXXXY syndrome. Clinical and psychological follow-up data.
Borghgraef M; Fryns JP; Smeets E; Marien J; van Den Berghe H
Clin Genet; 1988 Jun; 33(6):429-34. PubMed ID: 3168316
[TBL] [Abstract][Full Text] [Related]
10. [XXXXY syndrome: clinical-radiological findings in one patient (author's transl)].
Ventruto V; Pisciotta R; Celona A; Cavaliere ML; Pagano L; Stabile M; Fioretti G; Togo F
Radiol Med; 1981 Mar; 67(3):147-51. PubMed ID: 7268086
[TBL] [Abstract][Full Text] [Related]
11. The origin of telocentric chromosomes in man: a girl with tel(Xq).
Therman E; Sarto GE; DeMars RI
Hum Genet; 1981; 57(1):104-7. PubMed ID: 7262864
[TBL] [Abstract][Full Text] [Related]
12. 47,XXX chromosome constitution in a male.
Bigozzi U; Simoni G; Montali E; Dalpra L; Rossella F; Piazzini M; Borghi A
J Med Genet; 1980 Feb; 17(1):62-6. PubMed ID: 7189218
[TBL] [Abstract][Full Text] [Related]
13. XY translocation in a boy with ichthyosis, hypogonadism, short stature and mental retardation.
Matsumoto T; Taku K; Miike T; Harada N; Niikawa N
Clin Genet; 1991 Feb; 39(2):156-8. PubMed ID: 2015697
[No Abstract] [Full Text] [Related]
14. Fragile sites and X-linked retardation.
Hecht F; Hecht BK; Glover TW
Hosp Pract (Off Ed); 1981 Nov; 16(11):81-4, 86-8. PubMed ID: 6797930
[No Abstract] [Full Text] [Related]
15. 49 XXXXY syndrome with profound mental deficiency.
Christodorescu D; Constantinescu E; Ciovîrnache M; Costiner E
Neurol Psychiatr (Bucur); 1978; 16(2):79-84. PubMed ID: 684348
[No Abstract] [Full Text] [Related]
16. XXXXY syndrome in a phenotypic male infant with associated cardiac abnormalities.
Assemany SR; Neu RL; Gardner LI
Humangenetik; 1971; 12(2):101-4. PubMed ID: 5568728
[No Abstract] [Full Text] [Related]
17. 49,XXXXY: a distinct phenotype. Three new cases and review.
Peet J; Weaver DD; Vance GH
J Med Genet; 1998 May; 35(5):420-4. PubMed ID: 9610808
[TBL] [Abstract][Full Text] [Related]
18. The penta-X syndrome.
Monheit A; Francke U; Saunders B; Jones KL
J Med Genet; 1980 Oct; 17(5):392-6. PubMed ID: 7218280
[TBL] [Abstract][Full Text] [Related]
19. A duplication of distal Xp associated with hypogonadotrophic hypogonadism, hypoplastic external genitalia, mental retardation, and multiple congenital abnormalities.
Telvi L; Ion A; Carel JC; Desguerre I; Piraud M; Boutin AM; Feingold J; Ponsot G; Fellous M; McElreavey K
J Med Genet; 1996 Sep; 33(9):767-71. PubMed ID: 8880579
[TBL] [Abstract][Full Text] [Related]
20. Apparent homozygosity for the fragile site at Xq28 in a normal female.
Nielsen KB; Tommerup N; Poulsen H; Mikkelsen M
Hum Genet; 1982; 61(1):60-2. PubMed ID: 7129428
[No Abstract] [Full Text] [Related]
[Next] [New Search]