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 *

136 related articles for article (PubMed ID: 6496572)

  • 1. Brief clinical report: neural tube defects in dup(11q).
    Bader PI; Haney SM; Munsick RA; Schubert SR; Hodes ME
    Am J Med Genet; 1984 Sep; 19(1):5-8. PubMed ID: 6496572
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Familial balanced chromosome translocation t(12;13) in a family with several deformed stillbirths].
    Bommer C; Körner H
    Zentralbl Gynakol; 1982; 104(24):1578-83. PubMed ID: 6892078
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies.
    Elejalde BR; Opitz JM; de Elejalde MM; Gilbert EF; Abellera M; Meisner L; Lebel RR; Hartigan JM
    Am J Med Genet; 1984 Apr; 17(4):723-30. PubMed ID: 6539070
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Neural tube defects in chromosomally normal and abnormal human embryos.
    Coerdt W; Miller K; Holzgreve W; Rauskolb R; Schwinger E; Rehder H
    Ultrasound Obstet Gynecol; 1997 Dec; 10(6):410-5. PubMed ID: 9476327
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [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(3):293-300. PubMed ID: 7332142
    [No Abstract]   [Full Text] [Related]  

  • 7. Duplication of distal 11q and 22p occurrence in two unrelated families.
    Najafzadeh TM; Dumars KW
    Am J Med Genet; 1981; 8(3):341-7. PubMed ID: 7234904
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The dup(3q) syndrome: report of eight cases and review of the literature.
    Steinbach P; Adkins WN; Caspar H; Dumars KW; Gebauer J; Gilbert EF; Grimm T; Habedank M; Hansmann I; Herrmann J; Kaveggia EG; Langenbeck U; Meisner LF; Najafzadeh TM; Opitz JM; Palmer CG; Peters HH; Scholz W; Tavares AS; Wiedeking C
    Am J Med Genet; 1981; 10(2):159-77. PubMed ID: 7315873
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Trisomy (12p) with telocentric and pseudoisodicentric chromosome formation in a fetus.
    Plaja A; Mediano C; Farran I; Vendrell T; Toran N; Gili T; Sanchez MA; Sarret E
    Ann Genet; 1998; 41(1):52-5. PubMed ID: 9599652
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fetal hydrocephalus. Clinical significance of associated anomalies and genetic counseling: a pathological approach.
    Roume J; Larroche JC; Razavi-Encha F; Gonzales M; Migne G; Mulliez N
    Genet Couns; 1990; 1(3-4):185-96. PubMed ID: 2098043
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13).
    Tschernigg M; Petek E; Leonhardtsberger A; Wagner K; Kroisel PM
    Genet Couns; 2002; 13(3):303-7. PubMed ID: 12416638
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Chromosomal abnormalities associated with neural tube defects (II): partial aneuploidy.
    Chen CP
    Taiwan J Obstet Gynecol; 2007 Dec; 46(4):336-51. PubMed ID: 18182339
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Brief clinical report: the dup(17p) syndrome.
    Feldman GM; Baumer JG; Sparkes RS
    Am J Med Genet; 1982 Mar; 11(3):299-304. PubMed ID: 7081295
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Intrauterine diagnosis of a chromosome translocation].
    Aula P; Karjalainen O; Leisti J
    Duodecim; 1971; 87(20):1372-7. PubMed ID: 5115096
    [No Abstract]   [Full Text] [Related]  

  • 16. Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism.
    Habecker-Green JG; Naeem R; Gold H; O'Grady JP; Kanaan C; Bayer-Zwirello L; Murray MS; Cohn GM
    J Perinatol; 1998; 18(5):395-8. PubMed ID: 9766419
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q.
    Cousineau AJ; Higgins JV; Scott-Emuakpor AB; Mody G
    Am J Med Genet; 1983 Jan; 14(1):29-35. PubMed ID: 6829609
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Recombinant chromosome 18 in two offspring of a chromosome 18 inversion heterozygote.
    Andrews T; Gardiner AC; Boon AR
    Ann Genet; 1982; 25(3):185-8. PubMed ID: 6982674
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Genetic counseling and prenatal diagnosis in families with neural tube defects].
    Mikiel-Kostyra K
    Probl Med Wieku Rozwoj; 1983; 12():244-62. PubMed ID: 6674977
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.
    Xu J; Chernos J; Roland B
    Am J Med Genet; 1997 Dec; 73(3):327-9. PubMed ID: 9415693
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.