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 *

148 related articles for article (PubMed ID: 14227328)

  • 1. DEVELOPMENTAL RETARDATION ASSOCIATED WITH AN UNBALANCED 13-15/18 TRANSLOCATION.
    BREIBART S; MELLMAN WJ; EBERLEIN WR
    Cytogenetics; 1964; 3():252-7. PubMed ID: 14227328
    [No Abstract]   [Full Text] [Related]  

  • 2. A SMALL AUTOSOMAL RING CHROMOSOME IN A FEMALE INFANT WITH CONGENITAL MALFORMATIONS.
    LUCAS M; KEMP NH; ELLIS JR; MARSHALL R
    Ann Hum Genet; 1963 Nov; 27():189-95. PubMed ID: 14081490
    [No Abstract]   [Full Text] [Related]  

  • 3. [THE XXXXY SYNDROME].
    PRADER A; MUERSET G; HAUSCHTECK E
    Arch Kinderheilkd; 1964 Feb; 170():20-33. PubMed ID: 14163925
    [No Abstract]   [Full Text] [Related]  

  • 4. PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.
    VANDYKE HE; VALDMANIS A; MANN JD
    Am J Hum Genet; 1964 Sep; 16(3):364-74. PubMed ID: 14207551
    [No Abstract]   [Full Text] [Related]  

  • 5. Familial deletion of the short arm of the D1-chromosome (46, XX, 13 p-) not associated with loss of haptoglobin or catalase activity.
    Parker CE; Koch R; Mavalwala J; Derencsenyi A; Hatashita A
    Clin Pediatr (Phila); 1969 Aug; 8(8):453-8. PubMed ID: 5797429
    [No Abstract]   [Full Text] [Related]  

  • 6. Chromosomal anomalies in cryptorchidism and hypospadias.
    Yamaguchi T; Kitada S; Osada Y
    Urol Int; 1991; 47(2):60-3. PubMed ID: 1686509
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A retarded child with a 46XX,3p-q+ chromosome karyotype.
    Butler LJ; Hall ME; Wharton BA
    J Ment Defic Res; 1974 Mar; 18(0):41-9. PubMed ID: 4424443
    [No Abstract]   [Full Text] [Related]  

  • 8. Mental retardation with facial abnormalities, broad thumbs and toes and unusual dermatoglyphics.
    Davison BC; Ellis HL; Kuzemko JA; Roberts DF
    Dev Med Child Neurol; 1967 Oct; 9(5):588-93. PubMed ID: 5587707
    [No Abstract]   [Full Text] [Related]  

  • 9. DELETION OF THE SHORT ARM OF CHROMOSOME 18.
    SUMMITT RL
    Cytogenetics; 1964; 3():201-6. PubMed ID: 14227324
    [No Abstract]   [Full Text] [Related]  

  • 10. Syndrome associated with a deficiency of part of the long arm of chromosome no. 18.
    Insley J
    Arch Dis Child; 1967 Apr; 42(222):140-6. PubMed ID: 4381584
    [No Abstract]   [Full Text] [Related]  

  • 11. ENLARGED CHROMOSOMAL SATELLITES ASSOCIATED WITH MENTAL RETARDATION AND DIGITAL ARCHES IN THREE GENERATIONS.
    JACOBSON TS; TISCHLER B; MILLER JR
    Ann Hum Genet; 1964 Sep; 28():21-6. PubMed ID: 14204849
    [No Abstract]   [Full Text] [Related]  

  • 12. Two cases with a C-group ring autosome.
    Atkins L; Pant SS; Hazard GW; Ouellette EM
    Ann Hum Genet; 1966 Jul; 30(1):1-6. PubMed ID: 5964028
    [No Abstract]   [Full Text] [Related]  

  • 13. [FAMILIAL SEGREGATION OF A 5-13 TRANSLOCATION DETERMINING PARTIAL MONOSOMY AND A TRISOMY OF THE SHORT ARM OF THE 5 CHROMOSOME: "CAT CRY" DISEASE AND ITS "RECEPROCAL"].
    LEJEUNE J; LAFOURCADE J; BERGER R; TURPIN R
    C R Hebd Seances Acad Sci; 1964 Jun; 258():5767-70. PubMed ID: 14161436
    [No Abstract]   [Full Text] [Related]  

  • 14. A FAMILY WITH A FUSION TRANSLOCATION.
    WENAR C; RUTTENBERG BA; MELLMAN WJ; COOKE MS
    J Ment Defic Res; 1964 Dec; 8():SUPPL:93-101. PubMed ID: 14248583
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. PARTIAL DELETION OF THE SHORT ARMS OF A CHROMOSOME OF THE 4-5 GROUP (DENVER).
    DYGGVE HV; MIKKELSEN M
    Arch Dis Child; 1965 Feb; 40(209):82-5. PubMed ID: 14259280
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. Twins, probably monozygotic: one mongoloid with 48 chromosomes, the other normal.
    Dekaban A
    Cytogenetics; 1965; 4(4):227-39. PubMed ID: 4222115
    [No Abstract]   [Full Text] [Related]  

  • 19. UNUSUAL DERMATOGLYPHIC PATTERNS ASSOCIATED WITH CHROMOSOMAL ABNORMALITIES.
    HOEFNAGEL D; BENIRSCHKE K; MAVALWALA J; BROWNHILL L
    J Ment Defic Res; 1963 Dec; 7():90-101. PubMed ID: 14086188
    [No Abstract]   [Full Text] [Related]  

  • 20. A NOTE ON THE DERMAL RIDGE CONFIGURATIONS.
    HOLT SB
    J Med Genet; 1964 Sep; 1(1):32-4. PubMed ID: 14205981
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.