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 *

127 related articles for article (PubMed ID: 1178259)

  • 1. [Proceedings: Familial translocation 8-12 and the multiple abnormalities syndrome].
    Cousin J; Savary JB; Bayart M; Pauli A; Deminatti M; Fournier A
    Pediatrie; 1975; 30(3):314. PubMed ID: 1178259
    [No Abstract]   [Full Text] [Related]  

  • 2. Familial partial trisomy of the long arm of chromosome 10 (q24-26).
    Moreno-Fuenmayor H; Zackai EH; Mellman WJ; Aronson M
    Pediatrics; 1975 Nov; 56(5):756-61. PubMed ID: 1196732
    [TBL] [Abstract][Full Text] [Related]  

  • 3. De novo X;Y translocation associated with imperforate anus and retinal pigmentary abnormalities.
    Johnston K; Schonberg S; Littman V; Gregory T; Gelbart S; O'Donnell J; Cox DR
    Am J Med Genet; 1987 Jul; 27(3):603-11. PubMed ID: 3631132
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Iris transillumination defects associated with pallister-killian syndrome.
    Ticho BH
    J Pediatr Ophthalmol Strabismus; 2010; 47(1):58-9. PubMed ID: 20128558
    [TBL] [Abstract][Full Text] [Related]  

  • 5. D1 ring chromosome in newborn with peculiar face, polydactyly, imperforate anus, arrhinencephaly, and other malformations.
    Biles AR; Lüers T; Sperling K
    J Med Genet; 1970 Dec; 7(4):399-401. PubMed ID: 5501707
    [No Abstract]   [Full Text] [Related]  

  • 6. [Lethal polymalformative syndrome with 13q deletion secondary to a maternal X; 13 translocation].
    Vittu G; Croquette MF; Donney A; Duminy FR; Couturier J; Cousin J
    J Genet Hum; 1989 Jun; 37(2):141-7. PubMed ID: 2746173
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Townes-Brocks syndrome in an infant with translocation t (5;16).
    Serville F; Lacombe D; Saura R; Billeaud C; Sergent MP
    Genet Couns; 1993; 4(2):109-12. PubMed ID: 8357560
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Inverted duplication of 22pter----q11.21 in cat-eye syndrome.
    Hoo JJ; Robertson A; Fowlow SB; Bowen P; Lin CC
    Am J Med Genet; 1986 Jul; 24(3):543-5. PubMed ID: 3728573
    [No Abstract]   [Full Text] [Related]  

  • 9. The dup(3)(p25 leads to pter) syndrome: a case with holoprosencephaly.
    Martin NJ; Steinberg BG
    Am J Med Genet; 1983 Apr; 14(4):767-72. PubMed ID: 6846406
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recognizable patterns of human malformation.
    Smith DW
    Major Probl Clin Pediatr; 1976; 7():1-497. PubMed ID: 940360
    [No Abstract]   [Full Text] [Related]  

  • 11. Pallister-Killian syndrome: a report of 2 cases and review of its surgical aspects.
    Baglaj M; King J; Carachi R
    J Pediatr Surg; 2008 Jun; 43(6):1218-21. PubMed ID: 18558213
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Further delineation of the dup(3q) syndrome.
    Wilson GN; Dasouki M; Barr M
    Am J Med Genet; 1985 Sep; 22(1):117-23. PubMed ID: 4050847
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cat-eye syndrome: evaluation of the extra chromosome with banding techniques. Case report.
    De Chieri R; Malfatti C; Stanchi F; Albores JM
    J Genet Hum; 1974 Jun; 22(2):101-7. PubMed ID: 4213897
    [No Abstract]   [Full Text] [Related]  

  • 14. [A case of multiple congenital anomalies with familial C-G translocation].
    Yanagisawa S; Adachi K
    Jinrui Idengaku Zasshi; 1970 Mar; 14(4):309-15. PubMed ID: 5464693
    [No Abstract]   [Full Text] [Related]  

  • 15. [Monosomy C with mosaicism and thymic dysplasia].
    Bigliocchi A; Mattioli P; Ciarla MV; Madonna V
    Pediatria (Napoli); 1976 Jun; 84(2):307-19. PubMed ID: 1018997
    [No Abstract]   [Full Text] [Related]  

  • 16. [Extra mini-chromosome with symptoms of cat-eye syndrome].
    Méhes K; Bajnóczky K; Schmidt P
    Orv Hetil; 1985 Apr; 126(17):1037-9. PubMed ID: 3991187
    [No Abstract]   [Full Text] [Related]  

  • 17. A case of Aarskog syndrome with a review of Japanese literature.
    Aihara K; Nishi Y; Usui T
    Hiroshima J Med Sci; 1982 Jun; 31(2):87-90. PubMed ID: 7129954
    [No Abstract]   [Full Text] [Related]  

  • 18. [Bilateral anophthalmos. Facial anomalies and t(4;14) translocation].
    Serville F; Broustet A; Peyresblanques J; Bouineau J
    J Genet Hum; 1974 Dec; 22(4):341-51. PubMed ID: 4461763
    [No Abstract]   [Full Text] [Related]  

  • 19. Familial segregation of cervical ribs, Sprengel anomaly, preaxial polydactyly, anal atresia, and urethral obstruction: a new syndrome?
    Frydman M; Cohen HA; Ashkenazi A; Varsano I
    Am J Med Genet; 1993 Mar; 45(6):717-20. PubMed ID: 8456850
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Atypical cat eye syndrome. Fluorescence in situ hybridization of metaphase chromosomes].
    Bartsch O; Aksu F; Fenner A; Schwinger E
    Monatsschr Kinderheilkd; 1992 Aug; 140(8):460-3. PubMed ID: 1359403
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.