These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 3168316)

  • 1. 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]  

  • 2. 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]  

  • 3. Oral and dental development in X chromosome aneuploidy.
    Farge P; Dallaire L; Albert G; Melançon SB; Potier M; Leboeuf G
    Clin Genet; 1985 Feb; 27(2):122-6. PubMed ID: 3978846
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 49,XXXXY syndrome: behavioural and developmental profiles.
    Lomelino CA; Reiss AL
    J Med Genet; 1991 Sep; 28(9):609-12. PubMed ID: 1956059
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The 49,XXXXY syndrome: clinical and psychological findings in five patients.
    Curfs LM; Schreppers-Tijdink G; Wiegers A; Borghgraef M; Fryns JP
    J Ment Defic Res; 1990 Jun; 34 ( Pt 3)():277-82. PubMed ID: 2380984
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Molecular genetic analysis of a patient with moderate hemophilia A and psychomotor developmental delay.
    Gothwal M; Nakamura L; Hainmann I; Koehler U; Schilling F; Rost S; Oldenburg J; Zieger B
    Klin Padiatr; 2013 May; 225(3):175-6. PubMed ID: 23709133
    [No Abstract]   [Full Text] [Related]  

  • 11. [Case of chromosome X pentasomy].
    Sito A; Krzyzanowska J; Hofman H; Witkowska J; Sioch R; Mroczek-Orłow T
    Pediatr Pol; 1980 Jan; 55(1):77-80. PubMed ID: 7367071
    [No Abstract]   [Full Text] [Related]  

  • 12. Fragile (X) syndrome: a study of the psychological profile in 23 prepubertal patients.
    Borghgraef M; Fryns JP; Dielkens A; Pyck K; Van den Berghe H
    Clin Genet; 1987 Sep; 32(3):179-86. PubMed ID: 3621665
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [49 XXXXY syndrome. Description of 2 clinical cases].
    Verotti A; Chiarelli F; Violante N; Pellegrini E; Palka G
    Pediatr Med Chir; 1986; 8(4):575-8. PubMed ID: 3575135
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Case of XXXXY syndrome. Development throughout adolescence and endocrine aspects.
    Dötsch J; Foerster W; Holl R; Rascher W; Kiess W
    Horm Res; 2000; 53(3):154-6. PubMed ID: 11044797
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An XXYY male with schizophrenia.
    Lee JW
    Aust N Z J Psychiatry; 1996 Aug; 30(4):553-6. PubMed ID: 8887709
    [TBL] [Abstract][Full Text] [Related]  

  • 17. X chromosome abnormalities and cognitive development: implications for understanding normal human development.
    Walzer S
    J Child Psychol Psychiatry; 1985 Mar; 26(2):177-84. PubMed ID: 3884639
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Serologic explanation of the origin of the supernumerary X-chromosome in the XXXXY-syndrome].
    Murken JD; Scholz W
    Blut; 1967 Dec; 16(3):164-8. PubMed ID: 4384195
    [No Abstract]   [Full Text] [Related]  

  • 19. Partial trisomy 9q due to maternal 9/17 translocation.
    Aftimos SF; Hoo JJ; Parslow MI
    Am J Dis Child; 1980 Sep; 134(9):848-50. PubMed ID: 7416109
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.