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 *

114 related articles for article (PubMed ID: 4652494)

  • 1. [Trisomy of the chromosome 18 in a mentally retarded child with hyperphenylalaninemia].
    Adámek R; Zahálková M; Podhradská O; Saxl O; Mrskos A
    Acta Paediatr Acad Sci Hung; 1972; 13(1):33-7. PubMed ID: 4652494
    [No Abstract]   [Full Text] [Related]  

  • 2. Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22).
    Bowen P; Fitzgerald PH; Gardner RJ; Biederman B; Veale AM
    Am J Med Genet; 1983 Apr; 14(4):635-46. PubMed ID: 6846399
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An additional case of partial trisomy 18.
    Jenkins EC; Weed RG; Sandstrom MM
    Ann Genet; 1974 Mar; 17(1):45-8. PubMed ID: 4546345
    [No Abstract]   [Full Text] [Related]  

  • 4. Phenotypic overlapping of autosomal trisomy syndromes and its significance.
    Balakrishnan S; Puri RK; Bhargava I
    Indian Pediatr; 1971 Jul; 8(7):336-41. PubMed ID: 5113591
    [No Abstract]   [Full Text] [Related]  

  • 5. [Phenocopy of trisomy 18].
    Hongre JF; Toursei F; Staquet MF; Farriaux JP; Walbaum R
    Ann Pediatr (Paris); 1972 Nov; 19(11):825-30. PubMed ID: 4641249
    [No Abstract]   [Full Text] [Related]  

  • 6. [Trisomy 21 and trisomy 18 in siblings].
    Girardet P; Grosset L; Juillard E
    Helv Paediatr Acta; 1972 Dec; 27(6):583-9. PubMed ID: 4265243
    [No Abstract]   [Full Text] [Related]  

  • 7. The Edwards-Smith syndrome in a newborn girl.
    Guschina LA; Petrova SP; Bokarius LV
    Sov Genet; 1974 Oct; 8(11):1471-2. PubMed ID: 4445910
    [No Abstract]   [Full Text] [Related]  

  • 8. [Autosomal chromosome aberrations].
    Serville F; Battin J
    Bord Med; 1971 May; 4(5):1373-416. PubMed ID: 5105683
    [No Abstract]   [Full Text] [Related]  

  • 9. [Cp trisomy: a new syndrome].
    Canu JM; Buentello L; Armendares S
    Ann Genet; 1971 Sep; 14(3):177-86. PubMed ID: 5315464
    [No Abstract]   [Full Text] [Related]  

  • 10. Trisomy E with multiple congenital anomalies.
    Biswas B; Heycock JB
    Br J Clin Pract; 1973 Jul; 27(7):269-70. PubMed ID: 4727309
    [No Abstract]   [Full Text] [Related]  

  • 11. [Trisomy 18].
    Berger R
    Nouv Presse Med; 1972 Mar; 1(11):745-8. PubMed ID: 5022253
    [No Abstract]   [Full Text] [Related]  

  • 12. [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]  

  • 13. Trisomy 20p due to a paternal reciprocal translocation.
    Funderburk SJ; Sparkes RS; Sparkes MC
    Ann Genet; 1983; 26(2):94-7. PubMed ID: 6604493
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A case of 22-trisomy mosaic.
    Osztovics M; Ivády G
    Acta Paediatr Acad Sci Hung; 1977; 18(3-4):197-200. PubMed ID: 613730
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial trisomy 7q in two siblings.
    Klasen M; Schmid M; Hansmann I; Grimm T
    Ann Genet; 1983; 26(2):100-2. PubMed ID: 6604481
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Apropos of trisomy 18 - a study of 4 observations].
    Gilgenkrantz S; Sapelier J; Thiriet M; Kahn C; Pierson M
    Ann Genet; 1967 Mar; 10(1):32-8. PubMed ID: 5300124
    [No Abstract]   [Full Text] [Related]  

  • 17. [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]  

  • 18. [Chromosomal studies in craniofacial abnormalities].
    Ahrens K
    HNO; 1967 Apr; 15(4):106-9. PubMed ID: 5592377
    [No Abstract]   [Full Text] [Related]  

  • 19. Chromosomal aberration involving a member of the D group in a mentally retarded child with multiple congenital anomalies.
    Giorgi PL; Paci A; Ceccarelli M; Vizzoni L
    Helv Paediatr Acta; 1967 Oct; 22(5):466-71. PubMed ID: 5595749
    [No Abstract]   [Full Text] [Related]  

  • 20. Partial trisomy of chromosome 18 (pter leads to q11): a discussion on the identification of the critical segment.
    San Martin V; Fernandez-Novoa C; Hevia A; Novales A; Fornell J; Galera H
    Ann Genet; 1981; 24(4):248-50. PubMed ID: 6977308
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.