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 *

105 related articles for article (PubMed ID: 2457332)

  • 1. Atypical Prader-Willi syndrome with severe developmental delay and emaciation.
    Miike T; Ogata T; Ohtani Y; Yamaguchi H; Yokoyama Y
    Brain Dev; 1988; 10(3):186-8. PubMed ID: 2457332
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 'Expanded' Prader-Willi syndrome in a boy with an unusual 15q chromosome deletion.
    Pauli RM; Meisner LF; Szmanda RJ
    Am J Dis Child; 1983 Nov; 137(11):1087-9. PubMed ID: 6637912
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A case of Prader Willi syndrome with del 15 (q11-->q13).
    Tunçman G; Tükün A; Yalaz K; Bökesoy I
    Turk J Pediatr; 1993; 35(4):333-6. PubMed ID: 8160287
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Deletion of chromosome 15pter-->q11.2 due to t(Y;15) in a boy with Prader-Willi syndrome.
    Qumsiyeh MB; Dalton JD; Gordon PL; Wilroy RS; Tharapel AT
    Am J Med Genet; 1992 Jan; 42(1):109-11. PubMed ID: 1308348
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prader-Willi syndrome with chromosome 15 interstitial deletion: report of one case.
    Hwu WL; Tsai WY; Lee JS; Wang PJ; Wang TR
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1991; 32(2):105-11. PubMed ID: 2063683
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A case of an atypically large proximal 15q deletion as cause for Prader-Willi syndrome arising from a de novo unbalanced translocation.
    Hickey SE; Thrush DL; Walters-Sen L; Reshmi SC; Astbury C; Gastier-Foster JM; Atkin J
    Eur J Med Genet; 2013 Sep; 56(9):510-4. PubMed ID: 23856564
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Deletions of proximal 15q without Prader-Willi syndrome.
    Greenberg F; Ledbetter DH
    Am J Med Genet; 1987 Dec; 28(4):813-20. PubMed ID: 3688019
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Kleine-Levin syndrome in a boy with Prader-Willi syndrome.
    Gau SF; Soong WT; Liu HM; Hou JW; Tsai WY; Chiu YN; Yeh YC; Wang PJ; Wang TR
    Sleep; 1996 Jan; 19(1):13-7. PubMed ID: 8650457
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A report of a patient with interstitial deletion of 15q22: further delineation of a new micro deletion syndrome.
    Phadke SR; Sharda S
    Am J Med Genet A; 2008 Aug; 146A(15):1999-2000. PubMed ID: 18627036
    [No Abstract]   [Full Text] [Related]  

  • 10. [Cytogenetic detection of Prader-Willi syndrome in infancy].
    Götz J; Krüger G; Westphal BC; Pelz L
    Kinderarztl Prax; 1989 May; 57(5):239-43. PubMed ID: 2747122
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Derivative Y chromosome resulting from a t(Y;15) (q12;q11.2) in a boy with Prader-Willi syndrome.
    Suzuki Y; Sasagawa I; Sawamura T; Ishigooka M; Kaneko H; Kubota Y; Nakada T
    Int Urol Nephrol; 1996; 28(6):797-800. PubMed ID: 9089049
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A neuropathological study of a case of the Prader-Willi syndrome with an interstitial deletion of the proximal long arm of chromosome 15.
    Hayashi M; Itoh M; Kabasawa Y; Hayashi H; Satoh J; Morimatsu Y
    Brain Dev; 1992 Jan; 14(1):58-62. PubMed ID: 1590529
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical features in a de novo interstitial deletion 15q13 to q15.
    Autio S; Pihko H; Tengström C
    Clin Genet; 1988 Nov; 34(5):293-8. PubMed ID: 3228997
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prader-Willi syndrome and Robertsonian translocations involving chromosome 15.
    Casamassima AC; Shapiro LR; Wilmot PL; Smith KB
    Clin Genet; 1991 Apr; 39(4):294-7. PubMed ID: 1817468
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria.
    Gunay-Aygun M; Schwartz S; Heeger S; O'Riordan MA; Cassidy SB
    Pediatrics; 2001 Nov; 108(5):E92. PubMed ID: 11694676
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prader-Willi syndrome with del(15)(q11,q13) associated with hepatoblastoma.
    Hashizume K; Nakajo T; Kawarasaki H; Iwanaka T; Kanamori Y; Tanaka K; Utuki T; Mishina J; Watanabe T
    Acta Paediatr Jpn; 1991 Dec; 33(6):718-22. PubMed ID: 1666244
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Two Prader-Willi/Angelman syndrome loci present in an isodicentric marker chromosome.
    Luke S; Verma RS; Giridharan R; Conte RA; Macera MJ
    Am J Med Genet; 1994 Jul; 51(3):232-3. PubMed ID: 7521122
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Interstitial 15q deletion without a classic Prader-Willi phenotype.
    Galán F; Aguilar MS; González J; Clemente F; Sánchez R; Tapia M; Moya M
    Am J Med Genet; 1991 Mar; 38(4):532-4. PubMed ID: 2063892
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A case with 47,XXY,del(15)(q11;q13) karyotype associated with Prader-Willi phenotype.
    Rego A; Coll MD; Regal M; Guitart M; Escudero T; García-Mayor RV
    Horm Res; 1997; 48(1):44-6. PubMed ID: 9195210
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Comparison of high resolution cytogenetics, fluorescence in situ hybridisation, and DNA studies to validate the diagnosis of Prader-Willi and Angelman's syndromes.
    Smith A; Prasad M; Deng ZM; Robson L; Woodage T; Trent RJ
    Arch Dis Child; 1995 May; 72(5):397-402. PubMed ID: 7618904
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.