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 *

139 related articles for article (PubMed ID: 5454713)

  • 41. An abnormal C-group chromosome in a child with severe growth retardation.
    Holmes LB; Atkins L
    J Pediatr; 1968 Jul; 73(1):119-23. PubMed ID: 5658619
    [No Abstract]   [Full Text] [Related]  

  • 42. [Abnormal C group chromosome in several members of the same family].
    Emerit I; Vernant P
    Humangenetik; 1968; 6(4):326-34. PubMed ID: 5713618
    [No Abstract]   [Full Text] [Related]  

  • 43. 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]  

  • 44. [Cytogenetic study of the poulation of an institution receiving severely mentally retarded children. Comparisons with the data of psychiatric examination].
    Midenet M; Noël B; Quack B
    Rev Neuropsychiatr Infant; 1970 Mar; 18(3):249-58. PubMed ID: 5422823
    [No Abstract]   [Full Text] [Related]  

  • 45. FAMILIAL MOSAICISM OF A CHROMOSOME 16 ABNORMALITY ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES.
    TIPS RL; SMITH GS; MEYER DL; PERKINS AL
    Am J Ment Defic; 1964 Nov; 69():330-40. PubMed ID: 14223550
    [No Abstract]   [Full Text] [Related]  

  • 46. [Clinical anatomic and histopathological study of ocular signs in 2 cases of mosaicism associated with autosomal 18-21 double trisomy].
    Laliam M; Laliam N; Ouadahi MS; Iles S; Ould Larbi L
    Bull Mem Soc Fr Ophtalmol; 1972; 85(0):83-90. PubMed ID: 4211332
    [No Abstract]   [Full Text] [Related]  

  • 47. Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability.
    Naoufal R; Legendre M; Couet D; Gilbert-Dussardier B; Kitzis A; Bilan F; Harbuz R
    Eur J Med Genet; 2016 Sep; 59(9):483-7. PubMed ID: 27452446
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Turner syndrome and Noonan's syndrome.
    Summitt RL
    J Pediatr; 1969 Jan; 74(1):155-6. PubMed ID: 5782821
    [No Abstract]   [Full Text] [Related]  

  • 49. 48,XXXY/49,XXXXY Mosaicism in a 4 month old infant.
    Severi F; Colombo A; Svilokos N; Lo Curto F; Zuffardi O
    Padiatr Padol; 1974; 9(1):34-9. PubMed ID: 4456259
    [No Abstract]   [Full Text] [Related]  

  • 50. RING CHROMOSOME MOSAICISM IN A SEVERELY SUBNORMAL CHILD WITH MULTIPLE CONGENITAL MALFORMATIONS.
    FISHER GW
    J Ment Defic Res; 1965 Mar; 9():39-50. PubMed ID: 14293781
    [No Abstract]   [Full Text] [Related]  

  • 51. Multiple anomalies associated with a small extra metacentric autosome.
    Mukherjee AB; Partington MW; Simpson NE; Walmsley KA
    J Med Genet; 1968 Dec; 5(4):329-34. PubMed ID: 5713649
    [No Abstract]   [Full Text] [Related]  

  • 52. CONGENITAL ASYMMETRY ASSOCIATED WITH DIPLOID-TRIPLOID MOSAICISM AND LARGE SATELLITES.
    FERRIER P; STALDER G; BAMATTER F; FERRIER S; BUEHLER E; KLEIN D
    Lancet; 1964 Jan; 1(7324):80-2. PubMed ID: 14075544
    [No Abstract]   [Full Text] [Related]  

  • 53. GONADAL DYSGENESIS DUE TO MOSAICISM OF AN X CHROMOSOME FRAGMENT.
    BECKER KL; HAYLES AB; ALBERT A
    Proc Staff Meet Mayo Clin; 1963 Sep; 38():422-6. PubMed ID: 14064415
    [No Abstract]   [Full Text] [Related]  

  • 54. The MASA syndrome: a new heritable mental retardation syndrome.
    Bianchine JW; Lewis RC
    Clin Genet; 1974; 5(4):298-306. PubMed ID: 4855169
    [No Abstract]   [Full Text] [Related]  

  • 55. Ring-1 chromosome, microcephalic dwarfism, and acute myeloid leukemia.
    Bobrow M; Emerson PM; Spriggs AI; Ellis HL
    Am J Dis Child; 1973 Aug; 126(2):257-60. PubMed ID: 4125054
    [No Abstract]   [Full Text] [Related]  

  • 56. [Interpretation of the karyotype characteristics of patients with developmental defects of the urogenital system].
    Kirillova EA; Rozovskiĭ IS
    Tsitol Genet; 1980; 14(1):55-9. PubMed ID: 7445073
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Chromosomal abnormalities in a girl with physical and mental maldevelopment.
    Subrt I; Hníková O
    Hum Hered; 1970; 20(3):252-9. PubMed ID: 5489883
    [No Abstract]   [Full Text] [Related]  

  • 58. Gene deletion and duplication effects on phenotype and gamma globulin levels.
    Rudd NL; Lamarche PH
    J Med Genet; 1971 Mar; 8(1):97-106. PubMed ID: 5098075
    [No Abstract]   [Full Text] [Related]  

  • 59. OVARIAN DYSGENESIS WITH SEXUAL DEVELOPMENT AND MENSTRUATION (XO-XX MOSAICISM).
    BECKER KL; BURGERT EO; ALBERT A
    Proc Staff Meet Mayo Clin; 1963 Aug; 38():367-73. PubMed ID: 14047427
    [No Abstract]   [Full Text] [Related]  

  • 60. Mosaicism for an extra small ring chromosome.
    Forabosco A; Guaraldi G; Baroncini A; Ferrari E; Bassi C
    Dev Med Child Neurol; 1980 Feb; 22(1):92-6. PubMed ID: 7358237
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.