BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 728584)

  • 1. Trisomy 18 in sibs and maternal chromosome 9 variant.
    Pauli RM; Pagon RA; Hall JG
    Birth Defects Orig Artic Ser; 1978; 14(6C):297-301. PubMed ID: 728584
    [No Abstract]   [Full Text] [Related]  

  • 2. Familial translocation t(8;14) with a case of tertiary trisomy, +14q-.
    Soudek D; Hunter P; O'Shaughnessy S; Simpson NE; Soudek V
    Birth Defects Orig Artic Ser; 1978; 14(6C):309-15. PubMed ID: 728586
    [No Abstract]   [Full Text] [Related]  

  • 3. Trisomy 11q(q21 leads to qter).
    Bader PI; Jansch M; Hoffman D; Palmer CG; Gerber H; Taylor G
    Birth Defects Orig Artic Ser; 1978; 14(6C):383-92. PubMed ID: 728594
    [No Abstract]   [Full Text] [Related]  

  • 4. [Apropos of trisomy 18 - a study of 4 observations].
    Gilgenkrantz S; Sapelier J; Thiriet M; Kahn C; Pierson M
    Ann Genet; 1967 Mar; 10(1):32-8. PubMed ID: 5300124
    [No Abstract]   [Full Text] [Related]  

  • 5. 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
    [No Abstract]   [Full Text] [Related]  

  • 6. Partial trisomy 7q.
    Vogel W; Siebers JW; Reinwein H
    Ann Genet; 1973 Dec; 16(4):277-80. PubMed ID: 4544093
    [No Abstract]   [Full Text] [Related]  

  • 7. [Maternal translocation t (1; 8; 15) and trisomy 8 qter in her daughter. Genetic counseling].
    Ballesta F; Fernández E; Milá M
    J Genet Hum; 1980 Sep; 28(3):361-6. PubMed ID: 7463035
    [No Abstract]   [Full Text] [Related]  

  • 8. An intersexual infant with an extra chromosome.
    Insley J; Rushton DI; Jones HW
    Ann Genet; 1968 Jun; 11(2):88-94. PubMed ID: 5303428
    [No Abstract]   [Full Text] [Related]  

  • 9. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
    Butomo IV; Prozorova MV; Khitrikova LE
    Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human chromosome analysis: methodology and applications.
    Larson L
    Am J Med Technol; 1983 Oct; 49(10):687-98. PubMed ID: 6228140
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Familial observation of partial trisomy 6, and probable partial monosomy 18q by parental translocation].
    D'Emma C; Crippa L; Delozier C; Michail E; Graber P
    J Genet Hum; 1982 Mar; 30(1):39-50. PubMed ID: 7130955
    [TBL] [Abstract][Full Text] [Related]  

  • 12. E trisomy phenotype associated with small metacentric chromosome and a familial Y-22 translocation.
    Dumars KW; Fialko G; Larson E
    Birth Defects Orig Artic Ser; 1976; 12(5):97-104. PubMed ID: 953249
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].
    Rethoré MO; Larget-Piet L; Abonyi D; Boeswillwald M; Berger R; Carpentier S; Cruveiller J; Dutrillau B; Lafourcade J; Penneau M; Lejeune J
    Ann Genet; 1970 Dec; 13(4):217-32. PubMed ID: 5313386
    [No Abstract]   [Full Text] [Related]  

  • 14. An unbalanced karyotype in a translocation (Cq-,Aq+) pedigree.
    Smith GF; Shear CS; Jalowayski I; Akesson HO
    J Ment Defic Res; 1969 Jun; 13(2):123-9. PubMed ID: 5794286
    [No Abstract]   [Full Text] [Related]  

  • 15. Partial trisomy 13 due to maternal translocation t(7;13)(p22q14).
    Martin-Lucas MA; Pérez-Castillo A; Abrisqueta JA; de Torres ML; Martin-Sempere MJ; Del Mazo J; Aller V
    Ann Genet; 1982; 25(3):172-8. PubMed ID: 6982670
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial trisomy for different segments of chromosome 13 in several individuals of the same family.
    Wilroy RS; Summitt RL; Martens PR
    Birth Defects Orig Artic Ser; 1975; 11(5):217-22. PubMed ID: 1218217
    [No Abstract]   [Full Text] [Related]  

  • 17. [Partial trisomy 18 (pter leads to q122) of maternal origin (author's transl)].
    Jaffray JY; Geneix A; Goumy P; Perissel B; Menut G; Malet P
    Ann Genet; 1980; 23(4):224-7. PubMed ID: 6971601
    [TBL] [Abstract][Full Text] [Related]  

  • 18. High-resolution cytogenetics.
    Yunis JJ; Lewandowski RC
    Birth Defects Orig Artic Ser; 1983; 19(5):11-37. PubMed ID: 6309269
    [No Abstract]   [Full Text] [Related]  

  • 19. Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9.
    Butler LJ; Eades SM; France NE
    Ann Genet; 1969 Mar; 12(1):15-27. PubMed ID: 5306708
    [No Abstract]   [Full Text] [Related]  

  • 20. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation].
    Fioretti G; Pagano L; Renda S; Festa B; Rinaldi A; Celona A; Casullo C; Stabile M; Cavaliere ML; Ventruto V
    Minerva Pediatr; 1980 Jun; 32(12):807-14. PubMed ID: 7464734
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.