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 *

208 related articles for article (PubMed ID: 797303)

  • 1. [Interstitial deletion of the long arm of chromosome 7 in a female child with leprechaunism].
    Ayraud N; Rovinski J; Lambert JC; Galiana A
    Ann Genet; 1976 Dec; 19(4):265-8. PubMed ID: 797303
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Interstitial deletion of the long arm of one 11 chromosome].
    Taillemite JL; Morlier BG; Roux C
    Ann Genet; 1975 Mar; 18(1):61-3. PubMed ID: 1080039
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An abnormal metacentric chromosome in an infant with leprechaunism.
    Ferguson-Smith MA; Hamilton W; Ferguson IC; Ellis PM
    Ann Genet; 1968 Dec; 11(4):195-200. PubMed ID: 5306360
    [No Abstract]   [Full Text] [Related]  

  • 4. Partial deletion of the short arm of chromosome 12(p11; p13). Report of a case.
    Tenconi R; Baccichetti C; Anglani F; Pellergrino PA; Kaplan JC; Junien C
    Ann Genet; 1975 Jun; 18(2):95-8. PubMed ID: 1081371
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Interstitial deletion of the long arm of chromosome 11.
    Carnevale A; Blanco B; Grether P; Castillejos AR
    Ann Genet; 1987; 30(1):56-8. PubMed ID: 3498432
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome.
    Alfi O; Donnell GN; Crandall BF; Derencsenyi A; Menon R
    Ann Genet; 1973 Mar; 16(1):17-22. PubMed ID: 4541805
    [No Abstract]   [Full Text] [Related]  

  • 7. Chromosome 11 long arm partial deletion: a new syndrome.
    Engel E; Hirshberg CS; Cassidy SB; McGee BJ
    Am J Ment Defic; 1976 Jan; 80(4):473-5. PubMed ID: 1247044
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Long arm deletion of chromosome no. 6 in a mentally retarded boy with multiple physical malformations.
    Milosević J; Kalicanin P
    J Ment Defic Res; 1975 Jun; 19(2):139-44. PubMed ID: 1195357
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
    Destiné ML; Punnett HH; Thovichit S; DiGeorge AM; Weiss L
    Ann Genet; 1967 Jun; 10(2):65-9. PubMed ID: 5298975
    [No Abstract]   [Full Text] [Related]  

  • 10. Deletions of the long arm of chromosome 10.
    Shapiro SD; Hansen KL; Pasztor LM; DiLiberti JH; Jorgenson RJ; Young RS; Moore CM
    Am J Med Genet; 1985 Jan; 20(1):181-96. PubMed ID: 3970071
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q.
    Cousineau AJ; Higgins JV; Scott-Emuakpor AB; Mody G
    Am J Med Genet; 1983 Jan; 14(1):29-35. PubMed ID: 6829609
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The 9p- syndrome.
    Alfi OS; Donnell GN; Allderdice PW; Derencsenyi A
    Ann Genet; 1976 Mar; 19(1):11-6. PubMed ID: 1084115
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Partial deletion of the long arm of a group D (13-15) chromosome :Dq-].
    Laurent C; Cotton JB; Nivelon A; Freycon MT
    Ann Genet; 1967 Mar; 10(1):25-31. PubMed ID: 5300123
    [No Abstract]   [Full Text] [Related]  

  • 14. [4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].
    Rethoré MO; Larget-Piet L; Abonyi D; Boeswillwald M; Berger R; Carpentier S; Cruveiller J; Dutrillau B; Lafourcade J; Penneau M; Lejeune J
    Ann Genet; 1970 Dec; 13(4):217-32. PubMed ID: 5313386
    [No Abstract]   [Full Text] [Related]  

  • 15. Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature.
    Taysi K; Strauss AW; Yang V; Padmalatha C; Marshall RE
    Ann Genet; 1982; 25(3):141-4. PubMed ID: 6982660
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9.
    Butler LJ; Eades SM; France NE
    Ann Genet; 1969 Mar; 12(1):15-27. PubMed ID: 5306708
    [No Abstract]   [Full Text] [Related]  

  • 17. Interstitial deletion of the long arm of chromosome 2 in a malformed infant with karyotype 46,XX,del(2)(q31q33).
    Benson K; Gordon M; Wassman ER; Tsi C
    Am J Med Genet; 1986 Nov; 25(3):405-11. PubMed ID: 3789004
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deletion of 11q: report of two cases and a review.
    Larson SA; Yeatman GW; Riccardi VM
    Birth Defects Orig Artic Ser; 1976; 12(5):125-30. PubMed ID: 953212
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The child with congenital anomalies and interstitial deletion of the long arm of chromosome 4.
    Lech H; Kubalska J; Wisńiewski L
    Klin Padiatr; 1982 Mar; 194(2):117-9. PubMed ID: 7098371
    [No Abstract]   [Full Text] [Related]  

  • 20. A case of chromosome abnormality (46, XX, Gq+) with congenital heart disease and leprechaunism.
    Iwaski H; Abe M; Nawate G; Kato H
    Jinrui Idengaku Zasshi; 1974 Jun; 19(1):82-3. PubMed ID: 4476865
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.