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Journal Abstract Search

200 related items for PubMed ID: 4026150

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  • 6. A pedigree of 4/18 translocation chromosomes with type and countertype partial trisomy and partal monosomy for chromosome 18.
    Valdmanis A, Pearson G, Siegel AE, Hoeksema RH, Mann JD.
    Ann Genet; 1967 Dec; 10(4):159-66. PubMed ID: 5301688
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  • 10. Trisomy 3q2 and Pierre-Robin sequence in a boy with unbalanced 46,XY, der(10), t(3;10)(q23;q26.3) de novo karyotype.
    Kleczkowska A, Fryns JP, Moerman F, Martens M, Eggermont E, Jaeken J, Van den Berghe H.
    Helv Paediatr Acta; 1988 Nov; 43(3):245-8. PubMed ID: 3220792
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  • 13. Prenatal diagnosis of a 5/15 translocation with 5p and proximal 5q trisomy. Cytogenetic and phenotypic findings.
    Crowder WE, Yeast JD, Falk RE.
    Birth Defects Orig Artic Ser; 1982 Nov; 18(3 Pt A):143-51. PubMed ID: 7126787
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  • 15. De novo balanced translocation: 46, XX, t(13;20)(q34;p 11).
    Marinescu DD, Cioltei A, Pop T, Ioan D, Maximilian C.
    Endocrinologie; 1978 Nov; 16(4):295-8. PubMed ID: 734345
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  • 16. Partial trisomy 16q in the son resulting from paternal 16/21 translocation.
    Kosanović M, Lopicić L, Diklić V, Nikolis J.
    Acta Med Iugosl; 1983 Nov; 37(4):335-40. PubMed ID: 6650222
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  • 20. [Trisomy 10 p. Apropos of a case caused by a maternal translocation].
    Stoll C, Willard D.
    Pediatrie; 1980 Nov; 35(3):251-5. PubMed ID: 7393692
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