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Journal Abstract Search

210 related items for PubMed ID: 5109598

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. A mentally retarded male with karyotype 47,XY, plus mar equal ?i (18p).
    Nielsen J, Hreidarsson AB, Berggreen S, Ried E, Tsuboi T, Saldaña-Garcia P.
    Ann Genet; 1974 Jun; 17(2):129-33. PubMed ID: 4547941
    [No Abstract] [Full Text] [Related]

  • 23.
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  • 24. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
    Destiné ML, Punnett HH, Thovichit S, DiGeorge AM, Weiss L.
    Ann Genet; 1967 Jun; 10(2):65-9. PubMed ID: 5298975
    [No Abstract] [Full Text] [Related]

  • 25. A new syndrome with ptosis, coloboma and mental retardation.
    Le Marec B, Odent S, Urvoy M.
    Genet Couns; 1992 Jun; 3(2):119-20. PubMed ID: 1642810
    [No Abstract] [Full Text] [Related]

  • 26. Mosaic supernumerary small ring chromosome.
    Fryns JP, van Herck G, van den Berghe H.
    J Genet Hum; 1981 Jun; 29(2):151-4. PubMed ID: 7328409
    [No Abstract] [Full Text] [Related]

  • 27. [Chromosome aberrations in abortions].
    Boué JG, Boué A, Lazar P.
    Ann Genet; 1967 Dec; 10(4):179-87. PubMed ID: 5301690
    [No Abstract] [Full Text] [Related]

  • 28. A ring chromosome (46,XY,13r) occurring in a family with a D-D translocation 13-,14-, t(13q 14q).
    Mikkelsen M, Niebuhr E.
    Ann Genet; 1969 Mar; 12(1):51-6. PubMed ID: 5306712
    [No Abstract] [Full Text] [Related]

  • 29. An infant with 45 chromosomes including a D-E (13-15-17-18) translocation chromosome.
    Borgaonkar DS, Mules E, Scott CI.
    Johns Hopkins Med J; 1971 May; 128(5):282-8. PubMed ID: 5556542
    [No Abstract] [Full Text] [Related]

  • 30. Frequency of chromosomal aberrations in newborn infants with multiple developmental defects.
    Chebotarev AN.
    Sov Genet; 1974 Sep 15; 8(10):1329-30. PubMed ID: 4439048
    [No Abstract] [Full Text] [Related]

  • 31. [Partial monosomy of a C group chromosome (Cp-)].
    Laurent C, Nivelon A, Hartman E, Guerrier G.
    Ann Genet; 1968 Dec 15; 11(4):231-5. PubMed ID: 5306365
    [No Abstract] [Full Text] [Related]

  • 32. [Partial trisomy 11q;22q (author's transl)].
    Benítez J, Ayuso C, García Aparicio J, Sáez E, Pérez Sotelo A, Bello MJ.
    An Esp Pediatr; 1981 Sep 15; 15(3):293-300. PubMed ID: 7332142
    [No Abstract] [Full Text] [Related]

  • 33. [Ring chromosome 18].
    Hooft C, Haentjens P, Orye E, Kluyskens P, D'Hont G.
    Acta Paediatr Belg; 1968 Sep 15; 22(2):69-88. PubMed ID: 5747161
    [No Abstract] [Full Text] [Related]

  • 34. A case of 18q- in a t(18q-;6p+) family.
    Jacobsen P, Mikkelsen M, Niebuhr E, de Grouchy J.
    Ann Genet; 1971 Mar 15; 14(1):41-8. PubMed ID: 5314293
    [No Abstract] [Full Text] [Related]

  • 35. [Autoradiographic studies on X-autosomal translocation in man: 45,X.15-,tan(15qZq+)+].
    Engel W, Vogel W, Reinwein H.
    Cytogenetics; 1971 Mar 15; 10(2):87-98. PubMed ID: 5098032
    [No Abstract] [Full Text] [Related]

  • 36.
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  • 37. [Phenotype and karyotype interrelationships in chromosomal diseases].
    Prokof'eva-Bel'govska, Grinberg KN, Revazov AA, Mikel'saar AV, Kuliev AM.
    Vestn Akad Med Nauk SSSR; 1973 Mar 15; 28(1):37-44. PubMed ID: 4797784
    [No Abstract] [Full Text] [Related]

  • 38.
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  • 39.
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  • 40.
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