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: 7203470)

  • 21. Application of new technics of chromosome identification to cytogenetic problems.
    Borgaonkar DS
    Birth Defects Orig Artic Ser; 1973 Jan; 9(1):171-82. PubMed ID: 4120145
    [No Abstract]   [Full Text] [Related]  

  • 22. [Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18].
    Vivarelli R; Paolieri M; Anichini C; Scarinci R; Berardi R; Rosaia L; Pucci L
    Boll Soc Ital Biol Sper; 1992 Apr; 68(4):263-9. PubMed ID: 1463601
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Chromosome anomalies in 136 couples with a history of recurrent abortions.
    Diedrich U; Hansmann I; Janke D; Opitz O; Probeck HD
    Hum Genet; 1983; 65(1):48-52. PubMed ID: 6642507
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Ring chromosome 2 in a child with growth failure and few congenital abnormalities.
    Vigfusson NV; Kapstafer KJ; Lloyd MA
    Am J Med Genet; 1980; 7(3):383-9. PubMed ID: 7468662
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The results of chromosome examinations in an institution for mental retardates in the Cape Province.
    Nelson MM; Smart RD
    S Afr Med J; 1982 Jul; 62(1):25-9. PubMed ID: 7089776
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Chromosome abnormalities in newborn children. Physical aspects.
    Nielsen J; Hansen KB; Sillesen I; Videbech P
    Hum Genet; 1981; 59(3):194-200. PubMed ID: 7199023
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cytogenetic investigations in cases of multiple developmental anomalies in children.
    Gajewska-Obel E; Gebala A; Rusin T; Rozynkowa O
    Pol Med Sci Hist Bull (1973); 1975; 15(4):473-8. PubMed ID: 1223834
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Low level mosaicism for a balanced 7;14 translocation in the father of an abnormal 7q+ child.
    Sciorra LJ; Schlenker E; Toke D; Brady-Yasbin S; Day-Salvatore D; Lee ML
    Am J Med Genet; 1992 Feb; 42(3):296-7. PubMed ID: 1536164
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A cytogenetic survey of 14,069 new born infants. II. Preliminary clinical findings on children with sex chromosome anomalies.
    Grant WW; Hamerton JL
    Clin Genet; 1976 Nov; 10(5):285-302. PubMed ID: 791541
    [No Abstract]   [Full Text] [Related]  

  • 30. ABC of clinical genetics. Chromosomal disorders II.
    Kingston HM
    BMJ; 1989 Mar; 298(6676):813-6. PubMed ID: 2523747
    [No Abstract]   [Full Text] [Related]  

  • 31. Chromosome abnormalities in children of mothers 40 years of age or more. A retrospective investigation of a six-year hospital material.
    Geisler C; Wulf HC; Philip J
    Hum Hered; 1974; 24(5-6):449-53. PubMed ID: 4282612
    [No Abstract]   [Full Text] [Related]  

  • 32. A case of mosaic trisomy 14 due to an isochromosome, i(14q).
    Ozawa N; Xu ZD; Soh K; Takabayashi T; Sato S; Yajima A; Suzuki M; Ikeuchi T; Tonomura A
    Jinrui Idengaku Zasshi; 1984 Mar; 29(1):69-76. PubMed ID: 6748330
    [No Abstract]   [Full Text] [Related]  

  • 33. A liveborn 69,XXX triploid. Origin, X chromosome activity and gene dosage.
    Maraschio P; Danesino C; Lo Curto F; Zuffardi O; Dalla Fior T; Pedrotti D
    Ann Genet; 1984; 27(2):96-101. PubMed ID: 6331797
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Isochromosome-formation in chromosome 9.
    Miller K; Arslan-Kirchner M
    Ann Genet; 1994; 37(2):78-81. PubMed ID: 7985983
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Similar chromosomal abnormalities in several retinoblastomas.
    Kusnetsova LE; Prigogina EL; Pogosianz HE; Belkina BM
    Hum Genet; 1982; 61(3):201-4. PubMed ID: 7173862
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Induction of distinctive chromosomal bands in selected human subjects with D, G, and Y chromosome anomalies.
    Kakati S; Sinha AK
    Hum Hered; 1973 Apr; 23(4):313-30. PubMed ID: 4130026
    [No Abstract]   [Full Text] [Related]  

  • 37. 45,X/47,XYY mosaicism.
    Mulcahy MT; Jenkyn J; Mackellar A
    J Med Genet; 1977 Jun; 14(3):218-21. PubMed ID: 881716
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Chromosomal diseases in children].
    Demidova IA
    Med Sestra; 1988 Sep; 47(9):31-4. PubMed ID: 3205133
    [No Abstract]   [Full Text] [Related]  

  • 39. X-autosome translocation in normal mother and effectively 21-monosomic daughter.
    Summitt RL; Martens PR; Wilroy RS
    J Pediatr; 1974 Apr; 84(4):539-46. PubMed ID: 4834247
    [No Abstract]   [Full Text] [Related]  

  • 40. Chromosome studies in in-vitro fertilization patients.
    Lange R; Johannson G; Engel W
    Hum Reprod; 1993 Apr; 8(4):572-4. PubMed ID: 8501188
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.