BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 6430085)

  • 1. Cyclopia and cebocephaly in two newborn infants with unbalanced segregation of a familial translocation rcp (1;7)(q32;q34).
    Schinzel A
    Am J Med Genet; 1984 May; 18(1):153-61. PubMed ID: 6430085
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dup(3)(p2----pter) in two families, including one infant with cyclopia.
    Gimelli G; Cuoco C; Lituania M; Cordone M; Aricò M; Bianchi E; Maraschio P; Zuffardi O
    Am J Med Genet; 1985 Feb; 20(2):341-8. PubMed ID: 3919583
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cyclopia as a result of an unbalanced familial translocation, rcp(7;18)(q34;q21).
    Smart RD; Ross J; Amann G; Nelson MM
    Am J Med Genet; 1986 Jun; 24(2):269-72. PubMed ID: 3087168
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Multiple skeletal familial abnormalities associated with balanced reciprocal translocation 2;8(q32;p13).
    Ventruto V; Pisciotta R; Renda S; Festa B; Rinaldi MM; Stabile M; Cavaliere ML; Esposito M
    Am J Med Genet; 1983 Dec; 16(4):589-94. PubMed ID: 6660251
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
    Shaffer LG; Spikes AS; Macha M; Dunn R
    J Reprod Med; 1996 May; 41(5):367-71. PubMed ID: 8725766
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A paternal balanced translocation [t(7;22)(q32;q13.3)] leading to reciprocal unbalanced karyotypes in two consecutive pregnancies.
    Zackowski JL; Raffel LJ; McDaniel LD; Schwartz S
    Ann Genet; 1990; 33(2):113-6. PubMed ID: 2241085
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3.
    Pollin TI; Dobyns WB; Crowe CA; Ledbetter DH; Bailey-Wilson JE; Smith AC
    Am J Med Genet; 1999 Aug; 85(4):369-75. PubMed ID: 10398263
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A further case of cyclopia due to unbalanced segregation of a previously reported rcp(1;7)(q32;q34) familial translocation.
    Schinzel A
    Am J Med Genet; 1986 May; 24(1):205-6. PubMed ID: 3706408
    [No Abstract]   [Full Text] [Related]  

  • 9. Identical multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to del(2)(q32) in two sisters with intrachromosomal insertional translocation in their father.
    Pai GS; Rogers JF; Sommer A
    Am J Med Genet; 1983 Jan; 14(1):189-95. PubMed ID: 6829607
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 8q22-->qter duplication in a child with multiple congenital malformations: case report.
    Sasiadek M; Stembalska A; Schlade K; Zych M
    Med Sci Monit; 2000; 6(1):141-4. PubMed ID: 11208302
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial t(4;13) with abnormal offspring in three generations.
    Najafzadeh TM; Littman VA; Dumars KW
    Am J Med Genet; 1983 Sep; 16(1):15-22. PubMed ID: 6638065
    [TBL] [Abstract][Full Text] [Related]  

  • 12. High risk for unbalanced segregation of some reciprocal translocations: a large pedigree containing distal 4q trisomy from t(4;7)(q28;p22).
    Francisco-Bagnariolli AM; Payão SL; Kawasaki-Oyama RS; Sabbag Filho D; Segato R; de Labio RW; Chauffaille ML; Priest JH
    Am J Med Genet; 2001 Nov; 103(4):302-7. PubMed ID: 11746010
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Segregation patterns and phenotypes of unbalanced offspring in a large family with (10;18) chromosome translocation.
    Bernstein R; Pinto MR; Kromberg J; Wagner J; Jenkins T
    Am J Med Genet; 1985 Dec; 22(4):727-42. PubMed ID: 4073123
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chromosome 7 abnormalities in parents of children with holoprosencephaly and hydronephrosis.
    Lurie IW; Ilyina HG; Podleschuk LV; Gorelik LB; Zaletajev DV
    Am J Med Genet; 1990 Feb; 35(2):286-8. PubMed ID: 2309771
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and cytogenetic studies in a large (4;8) translocation family with pre- and postnatal Wolf syndrome.
    Tranebjaerg L; Petersen A; Hove K; Rehder H; Mikkelsen M
    Ann Genet; 1984; 27(4):224-9. PubMed ID: 6335368
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial 3q trisomy due to an unbalanced 3/10 translocation.
    Blumberg B; Moore R; Mohandas T
    Am J Med Genet; 1980; 7(3):335-9. PubMed ID: 7468658
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the Down syndrome.
    Kitsiou-Tzeli S; Hallett JJ; Atkins L; Latt SA; Holmes LB
    Am J Med Genet; 1984 Aug; 18(4):725-9. PubMed ID: 6237580
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Variable expression of phenotype in offspring with partial monosomy 7q and partial trisomy 8p in a family with a rcp (7;8)(134;p12) translocation.
    Frints SG; Moerman P; Fryns JP
    Genet Couns; 1996; 7(4):313-9. PubMed ID: 8985736
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inheritance of a translocation between chromosomes 12 and 16 in a family with recurrent miscarriages and a newborn with Down syndrome carrying the same translocation.
    Pazarbaşi A; Demirhan O; Turgut M; Güzel I; Taştemir D
    Genet Couns; 2008; 19(3):301-8. PubMed ID: 18990986
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial translocation, t(2;5) (p23; g31).
    Osztovics M; Kiss P
    Clin Genet; 1975 Aug; 8(2):112-6. PubMed ID: 1175316
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.