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 *

121 related articles for article (PubMed ID: 2369068)

  • 1. [Cri-du-chat disease: plasma and urinary amino acids].
    Lejeune J; Rethoré MO; Peeters M; de Blois MC; Rabier D; Parvy P; Bardet J; Kamoun P
    Ann Genet; 1990; 33(1):16-20. PubMed ID: 2369068
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Metabolic anomalies in cri du chat syndrome (5p-) lymphocytes and de novo purine synthesis.
    Peeters MA; Rethoré MO; Aris L; Megarbane A; Cattaneo F; Lejeune J
    Ann Genet; 1991; 34(3-4):219-25. PubMed ID: 1809230
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Oxygen consumption of leukocytes in chromosome abnormalities. (Down's syndrome, ring chromosome 21, cri-du-chat syndrome, trisomy 18 and 22)].
    Heyne K
    Med Welt; 1980 Feb; 31(7):251-4. PubMed ID: 6445033
    [No Abstract]   [Full Text] [Related]  

  • 4. Ocular findings in a patient with deletion short arm chromosome 5 (cri du chat) and ring chromosome 14.
    Clark DI; Howard PJ; Patterson A
    Trans Ophthalmol Soc U K (1962); 1986; 105 ( Pt 6)():723-5. PubMed ID: 3477901
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Variability in a family with an insertion involving 5p.
    Marinescu RC; Mamunes P; Kline AD; Schmidt J; Rojas K; Overhauser J
    Am J Med Genet; 1999 Sep; 86(3):258-63. PubMed ID: 10482876
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A yeast artificial chromosome contig of the critical region for cri-du-chat syndrome.
    Goodart SA; Simmons AD; Grady D; Rojas K; Moyzis RK; Lovett M; Overhauser J
    Genomics; 1994 Nov; 24(1):63-8. PubMed ID: 7896290
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypic and phoniatric findings in mosaic cri du chat syndrome.
    Romano C; Ragusa RM; Scillato F; Greco D; Amato G; Barletta C
    Am J Med Genet; 1991 Jun; 39(4):391-5. PubMed ID: 1877615
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Mental retardation in the crying cat syndrome. Comparison of the intellectual level in the partial deletion of the short arm of chromosome 5 with trisomy 21 and deletions of chromosome 18. Apropos of 118 cases taken from the literature].
    Moor L
    Rev Neuropsychiatr Infant; 1968 Mar; 16(3):257-67. PubMed ID: 5683042
    [No Abstract]   [Full Text] [Related]  

  • 9. Characterization of a complex chromosomal rearrangement in a patient with a typical catlike cry and no other clinical findings of cri-du-chat syndrome.
    Sreekantaiah C; Kronn D; Marinescu RC; Goldin B; Overhauser J
    Am J Med Genet; 1999 Sep; 86(3):264-8. PubMed ID: 10482877
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cri du chat mosaicism: an unusual case of partial deletion and partial deletion/ duplication of the short arm of chromosome 5, leading to an unusual cri du chat phenotype.
    Murru D; Boccone L; Ristaldi MS; Nucaro AL
    Genet Couns; 2008; 19(4):381-6. PubMed ID: 19239081
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.
    Harvard C; Malenfant P; Koochek M; Creighton S; Mickelson EC; Holden JJ; Lewis ME; Rajcan-Separovic E
    Clin Genet; 2005 Apr; 67(4):341-51. PubMed ID: 15733271
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cri du chat syndrome.
    Iyer SL; Duraiswamy A; Kher AS; Joshi S; Bharucha BA; Kanade S
    J Postgrad Med; 1996; 42(3):86-8. PubMed ID: 9715326
    [TBL] [Abstract][Full Text] [Related]  

  • 13. "Cri du chat" syndrome. Partial deletion of the short arm of a chromosome No. 5. Report of a case.
    Hustinx TW; Wijffels JC
    Maandschr Kindergeneeskd; 1965 Aug; 33(8):286-98. PubMed ID: 5848077
    [No Abstract]   [Full Text] [Related]  

  • 14. An autoradiographic study of the chromosomes in the cri du chat syndrome.
    Balícek P; Zizka J; Skalská H
    Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove; 1971; 14(4):405-12. PubMed ID: 5291170
    [No Abstract]   [Full Text] [Related]  

  • 15. The "cri du chat" syndrome.
    Mladkovskaya TB; Lebedev BV; Mazaeva IV
    Sov Genet; 1970 Oct; 6(10):1374-9. PubMed ID: 4272596
    [No Abstract]   [Full Text] [Related]  

  • 16. Cri du chat-syndrome in combination with partial trisomy 9 p.
    Sigmund J; Frisch H; Heinz-Erian P; Rhomberg K; Wegner RD
    Padiatr Padol; 1986; 21(1):61-7. PubMed ID: 3960564
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Cri-du-chat syndrome and two other deformed children in a family carrying a pericentric inversion or insertion of chromosome 5].
    Delozier-Blanchet CD; Pitmon D; Schorderet D; Engel E
    J Genet Hum; 1985 Dec; 33(5):371-80. PubMed ID: 4093767
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The intelligence level in the chromosome aberrations affecting autosomes].
    Moor L
    Rev Neuropsychiatr Infant; 1970 Dec; 18(12):943-66. PubMed ID: 4251821
    [No Abstract]   [Full Text] [Related]  

  • 19. [Deficiency of the short arm of chromosome. 5. Crying cat syndrome].
    Berger R
    Nouv Presse Med; 1972 Mar; 1(13):873-5. PubMed ID: 5018461
    [No Abstract]   [Full Text] [Related]  

  • 20. [Identification of 2 familial translocations].
    Laurent C; Biemont MC; Robert JM; Dutrillaux B
    Ann Genet; 1974 Dec; 17(4):279-81. PubMed ID: 4548825
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.