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 *

179 related articles for article (PubMed ID: 4429360)

  • 1. Chromosome studies in investigation of stillbirths and neonatal deaths.
    Bauld R; Sutherland GR; Bain AD
    Arch Dis Child; 1974 Oct; 49(10):782-8. PubMed ID: 4429360
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chromosome abnormality and perinatal death.
    Machin GA
    Lancet; 1974 Mar; 1(7857):549-51. PubMed ID: 4131984
    [No Abstract]   [Full Text] [Related]  

  • 3. Cytogenetic studies in perinatal death.
    Smith A; Bannatyne P; Russell P; Ellwood D; den Dulk G
    Aust N Z J Obstet Gynaecol; 1990 Aug; 30(3):206-10. PubMed ID: 2256858
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chromosome constitution of 500 infants dying during the perinatal period. With an appendix concerning other genetic disorders among these infants.
    Machin GA; Crolla JA
    Humangenetik; 1974; 23(3):183-98. PubMed ID: 4844640
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. Chromosome studies at the paediatric necropsy.
    Sutherland GR; Carter RF; Bauld R; Smith II; Bain AD
    Ann Hum Genet; 1978 Oct; 42(2):173-81. PubMed ID: 569457
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chromosome variation in perinatal mortality: a survey of 500 cases.
    Angell RR; Sandison A; Bain AD
    J Med Genet; 1984 Feb; 21(1):39-44. PubMed ID: 6229635
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chromosome studies in repeated spontaneous abortions and stillbirths.
    Pergament E; Kadotani T; Sato H
    Am J Obstet Gynecol; 1968 Apr; 100(7):912-7. PubMed ID: 5644302
    [No Abstract]   [Full Text] [Related]  

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

  • 10. Cytogenetics of pregnancy wastage.
    Boué A; Boué J; Gropp A
    Adv Hum Genet; 1985; 14():1-57. PubMed ID: 3887861
    [No Abstract]   [Full Text] [Related]  

  • 11. ACOG committee opinion. Genetic evaluation of stillbirths and neonatal deaths. Number 178, November 1996. Committee on Genetics. American College of Obstetricians and Gynecologists.
    Int J Gynaecol Obstet; 1997 Mar; 56(3):287-9. PubMed ID: 9127165
    [No Abstract]   [Full Text] [Related]  

  • 12. Trisomy 18 associated with a familial translocation t(Bq-; 18q+).
    France NE; Butler LJ
    Ann Genet; 1969 Mar; 12(1):46-50. PubMed ID: 5306711
    [No Abstract]   [Full Text] [Related]  

  • 13. Fetal and placenta chromosome constitution in 237 pregnancy losses.
    Baena N; Guitart M; Ferreres JC; Gabau E; Corona M; Mellado F; Egozcue J; Caballín MR
    Ann Genet; 2001; 44(2):83-8. PubMed ID: 11522246
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chromosome anomalies of infants dying during the perinatal period and premature newborn.
    Kuleshov NP
    Hum Genet; 1976 Feb; 31(2):151-60. PubMed ID: 129431
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Trisomy 18 in one of fraternal twins.
    Gertzer D; Nathenson G
    J Med Genet; 1971 Sep; 8(3):392-4. PubMed ID: 5097150
    [No Abstract]   [Full Text] [Related]  

  • 16. Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome.
    Taylor AI
    J Med Genet; 1968 Sep; 5(3):227-52. PubMed ID: 5708029
    [No Abstract]   [Full Text] [Related]  

  • 17. Trisomy 18 mosaicism in a woman with normal intelligence, pigmentary dysplasia, and an 18 trisomic daughter.
    Ukita M; Hasegawa M; Nakahori T
    Am J Med Genet; 1997 Jan; 68(2):240-1. PubMed ID: 9028467
    [No Abstract]   [Full Text] [Related]  

  • 18. Autosomal reciprocal translocations in newborn children and their relatives.
    Friedrich U; Nielsen J
    Humangenetik; 1974 Feb; 21(2):133-44. PubMed ID: 4135077
    [No Abstract]   [Full Text] [Related]  

  • 19. Frequency and occurrence of chromosomal syndromes. I. D-Trisomy.
    Conen PE; Erkman B
    Am J Hum Genet; 1966 Jul; 18(4):374-86. PubMed ID: 5945953
    [No Abstract]   [Full Text] [Related]  

  • 20. Extra-small marker chromosomes in couples with reproductive failure.
    Ioan D; Dumitriu L; Ghergar D; Belengeanu V; Soare GH; Maximilian C
    Endocrinologie; 1987; 25(1):41-3. PubMed ID: 3472313
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.