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 *

406 related articles for article (PubMed ID: 5782825)

  • 1. Cytogenetics in mentally defective children with anomalies: a controlled study.
    Summitt RL
    J Pediatr; 1969 Jan; 74(1):58-66. PubMed ID: 5782825
    [No Abstract]   [Full Text] [Related]  

  • 2. Trisomy 9 mosaicism with multiple congenital anomalies.
    Haslam RH; Broske SP; Moore CM; Thomas GH; Neill CA
    J Med Genet; 1973 Jun; 10(2):180-4. PubMed ID: 4714587
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromosome aberrations in 50 patients with idiopathic mental retardation and in 50 control subjects. Madison blind study 3.
    Daly RF
    J Pediatr; 1970 Sep; 77(3):444-53. PubMed ID: 5502094
    [No Abstract]   [Full Text] [Related]  

  • 4. A mentally retarded boy with multiple congenital anomalies and aberrant morphology in a no. 18 chromosome.
    Van Kempen C
    Dev Med Child Neurol; 1967 Oct; 9(5):617-24. PubMed ID: 6066027
    [No Abstract]   [Full Text] [Related]  

  • 5. An extra small metacentric chromosome in a mentally retarded boy.
    Ishmael J; Laurence KM
    J Med Genet; 1968 Dec; 5(4):335-40. PubMed ID: 5713650
    [No Abstract]   [Full Text] [Related]  

  • 6. An extra small metacentric chromosome in association with multiple congenital abnormalities.
    Finley WH; Finley SC; Monsky D
    J Med Genet; 1971 Sep; 8(3):381-3. PubMed ID: 5097148
    [No Abstract]   [Full Text] [Related]  

  • 7. A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter.
    Voss R; Gross-Kieselstein E; Hurvitz H; Dagan J; Kerem E; Zlotogora J
    J Med Genet; 1984 Dec; 21(6):454-9. PubMed ID: 6512835
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Tertiary trisomy in a human kindred containing an E/G translocation.
    Macintyre MN; Walden DB; Hempel JM
    Am J Hum Genet; 1971 Sep; 23(5):431-41. PubMed ID: 5092595
    [No Abstract]   [Full Text] [Related]  

  • 9. Autosomal chromosome aberrations in ophthalmology.
    François J
    J Neurol Sci; 1967; 4(3):511-58. PubMed ID: 4228074
    [No Abstract]   [Full Text] [Related]  

  • 10. Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.
    Sanchez O; Yunis JJ; Escobar JI
    Humangenetik; 1974 Apr; 22(1):59-65. PubMed ID: 4134840
    [No Abstract]   [Full Text] [Related]  

  • 11. Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.
    Sartori A; Tenconi R; Baccichetti C; Pujatti G
    Acta Paediatr Scand; 1974 Jul; 63(4):631-5. PubMed ID: 4850900
    [No Abstract]   [Full Text] [Related]  

  • 12. Ring chromosome 18 in a patient with multiple anomalies.
    Palmer CG; Fareed N; Merritt AD
    J Med Genet; 1967 Jun; 4(2):117-23. PubMed ID: 5619991
    [No Abstract]   [Full Text] [Related]  

  • 13. Tandem duplication (5q13 to 22) in a mentally deficient girl.
    Kessel E; Pfeiffer RA
    Hum Genet; 1979 Nov; 52(2):217-20. PubMed ID: 511177
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mental deficiency and malformations in a boy with a group-C ring chromosome: 46, XY, Cr.
    Wurster D; Pomeroy J; Benirschke K; Hoefnagel D
    J Ment Defic Res; 1969 Sep; 13(3):184-90. PubMed ID: 5823674
    [No Abstract]   [Full Text] [Related]  

  • 15. Trisomy D-trisomy E mosaicism in an infant male.
    Warren RJ; Keith JI
    J Med Genet; 1971 Sep; 8(3):384-6. PubMed ID: 5097149
    [No Abstract]   [Full Text] [Related]  

  • 16. A cytogenetic survey of an institution for the mentally retarded: I. Chromosome abnormalities.
    Jacobs PA; Matsuura JS; Mayer M; Newlands IM
    Clin Genet; 1978 Jan; 13(1):37-60. PubMed ID: 146575
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 46,XY-47,XY,C+ mosaicism in a male infant with multiple anomalies.
    Oikawa K; Kajii T; Shimba H; Sasaki M
    Ann Genet; 1969 Jun; 12(2):102-6. PubMed ID: 5308379
    [No Abstract]   [Full Text] [Related]  

  • 18. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
    Jacobsen P; Hauge M; Henningsen K; Hobolth N; Mikkelsen M; Philip J
    Hum Hered; 1973; 23(6):568-85. PubMed ID: 4134631
    [No Abstract]   [Full Text] [Related]  

  • 19. Cytogenetics of 50 patients with mental retardation and multiple congenital anomalies and 50 normal subjects. Madison blind study IV.
    Magnelli NC
    Clin Genet; 1976 Feb; 9(2):169-82. PubMed ID: 1248176
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pallister-Killian syndrome in older children and adolescents.
    Horneff G; Majewski F; Hildebrand B; Voit T; Lenard HG
    Pediatr Neurol; 1993; 9(4):312-5. PubMed ID: 8216546
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.