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 *

153 related articles for article (PubMed ID: 10071191)

  • 21. Autism and Williams syndrome: a case report.
    Herguner S; Mukaddes NM
    World J Biol Psychiatry; 2006; 7(3):186-8. PubMed ID: 16861145
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Molecular characterization of Xp chromosome deletion in a fertile cow.
    De Lorenzi L; Rossi E; Genualdo V; Gimelli S; Lasagna E; Perucatti A; Iannuzzi A; Parma P
    Sex Dev; 2012; 6(6):298-302. PubMed ID: 22964474
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular and cytogenetic studies of X inactivation in a patient with 46,X,del(X)(q22).
    Witchel SF; Wenger SL; Hoffman EP
    J Pediatr Adolesc Gynecol; 1997 May; 10(2):78-82. PubMed ID: 9179806
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions.
    Lachlan KL; Youings S; Costa T; Jacobs PA; Thomas NS
    Hum Genet; 2006 Jan; 118(5):640-51. PubMed ID: 16283387
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Del(X)(p21.1) in a mother and two daughters: genotype-phenotype correlation of Turner features.
    Adachi M; Tachibana K; Asakura Y; Muroya K; Ogata T
    Hum Genet; 2000 Mar; 106(3):306-10. PubMed ID: 10798359
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Novel chromosomal translocation t(11;9)(p15;p23) involving deletion and duplication of 9p in a girl associated with autism and mental retardation.
    Yang Y; Wang C; Wang F; Zhu L; Liu H; He X
    Gene; 2012 Jul; 502(2):154-8. PubMed ID: 22555022
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Random X inactivation resulting in mosaic nullisomy of region Xp21.1----p21.3 associated with heterozygosity for ornithine transcarbamylase deficiency and for chronic granulomatous disease.
    Francke U
    Cytogenet Cell Genet; 1984; 38(4):298-307. PubMed ID: 6510024
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements.
    Giglio S; Pirola B; Arrigo G; Dagrada P; Bardoni B; Bernardi F; Russo G; Argentiero L; Forabosco A; Carrozzo R; Zuffardi O
    Eur J Hum Genet; 2000 Jan; 8(1):63-70. PubMed ID: 10713889
    [TBL] [Abstract][Full Text] [Related]  

  • 29. X-chromosome workshop.
    Paterson AD
    Psychiatr Genet; 1998; 8(2):121-6. PubMed ID: 9686435
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The fragile X marker and autism in perspective.
    Payton JB; Steele MW; Wenger SL; Minshew NJ
    J Am Acad Child Adolesc Psychiatry; 1989 May; 28(3):417-21. PubMed ID: 2738009
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Short stature in a mother and daughter with terminal deletion of Xp22.3.
    Schwinger E; Kirschstein M; Greiwe M; Konermann T; Orth U; Gal A
    Am J Med Genet; 1996 May; 63(1):239-42. PubMed ID: 8723116
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure.
    Marozzi A; Manfredini E; Tibiletti MG; Furlan D; Villa N; Vegetti W; Crosignani PG; Ginelli E; Meneveri R; Dalprà L
    Hum Genet; 2000 Oct; 107(4):304-11. PubMed ID: 11129329
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation.
    Gustashaw KM; Zurcher V; Dickerman LH; Stallard R; Willard HF
    Am J Med Genet; 1994 Oct; 53(1):39-45. PubMed ID: 7802034
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Chromosome 7q: where autism meets language disorder?
    Folstein SE; Mankoski RE
    Am J Hum Genet; 2000 Aug; 67(2):278-81. PubMed ID: 10889044
    [No Abstract]   [Full Text] [Related]  

  • 36. Pigmentary mosaicism in hypomelanosis of Ito. Further evidence for functional disomy of Xp.
    Fritz B; Küster W; Orstavik KH; Naumova A; Spranger J; Rehder H
    Hum Genet; 1998 Oct; 103(4):441-9. PubMed ID: 9856488
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Isodicentric X chromosome in a patient with Turner syndrome--implications for localization of the X-inactivation center.
    Pettigrew AL; McCabe ER; Elder FF; Ledbetter DH
    Hum Genet; 1991 Aug; 87(4):498-502. PubMed ID: 1879836
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivation.
    Callen DF; Eyre HJ; Dolman G; Garry-Battersby MB; McCreanor JR; Valeba A; McGill JJ
    J Med Genet; 1995 Feb; 32(2):113-6. PubMed ID: 7760319
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses.
    Ballabio A; Andria G
    Hum Mol Genet; 1992 Jul; 1(4):221-7. PubMed ID: 1303191
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis.
    Therman E; Susman B
    Hum Genet; 1990 Jul; 85(2):175-83. PubMed ID: 2370045
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.