BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

233 related articles for article (PubMed ID: 6620332)

  • 21. A neuropsychological-genetic profile of atypical cri du chat syndrome: implications for prognosis.
    Cornish KM; Cross G; Green A; Willatt L; Bradshaw JM
    J Med Genet; 1999 Jul; 36(7):567-70. PubMed ID: 10424821
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Genetic analysis of a case with atypical neonatal Cri-du-chat syndrome].
    He W; Chen H; Mu H; Li J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb; 35(1):104-106. PubMed ID: 29419873
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [A de novo partial 5p deletion and cryptic 18p duplication detected by SNP-Array in a boy featuring Cri du Chat syndrome].
    Hu JC; Tan K; Cheng DH; Li LY; Lu GX; Tan YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):87-90. PubMed ID: 23450488
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 5p;12q translocation with manifestations of cri du chat syndrome and Marfanoid arachnodactyly.
    Zhang SZ; Tang YC; Dai FP; Niebuhr E
    Clin Genet; 1990 Feb; 37(2):153-7. PubMed ID: 2311266
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Transmission of the cri-du-chat syndrome from a maternal balanced translocation carrier, t(5p-;11q+).
    Singh DN; Osborne RA; Wiscovitch RA
    Humangenetik; 1973 Dec; 20(4):361-5. PubMed ID: 4768112
    [No Abstract]   [Full Text] [Related]  

  • 26. Partial translocation of NOR and its activity in a balanced carrier and in her cri-du-chat fetus.
    Dev VG; Byrne J; Bunch G
    Hum Genet; 1979 Oct; 51(3):277-80. PubMed ID: 511156
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the "cri du chat" syndrome.
    Faed MJ; Marrian VJ; Robertson J; Robson EB; Cook PJ
    Cytogenetics; 1972; 11(5):400-11. PubMed ID: 4119109
    [No Abstract]   [Full Text] [Related]  

  • 28. A case of cri-du-chat associated with cataracts and transmitted from a mother with a 4-5 translocation.
    Grotsky H; Hsu LY; Hirschhorn K
    J Med Genet; 1971 Sep; 8(3):369-71. PubMed ID: 5097145
    [No Abstract]   [Full Text] [Related]  

  • 29. [Prenatal diagnosis of the cri-du-chat syndrome in the case of balanced 5p--; 18p+ translocation in the mother].
    Zolotukhina TV; Butomo IV; Rozovskiĭ IS; Grinberg KN
    Genetika; 1981; 17(7):1304-8. PubMed ID: 7196856
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Fertility and the cri du chat syndrome.
    Martínez JE; Tuck-Muller CM; Superneau D; Wertelecki W
    Clin Genet; 1993 Apr; 43(4):212-4. PubMed ID: 8330455
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Cri-du-chat syndrome.
    Chang CY; Lin SP; Lin HY; Chen YJ; Kao HA; Yeung CY; Hsu CH; Chi H
    Acta Paediatr Taiwan; 2007; 48(6):328-31. PubMed ID: 18437967
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Prenatal detection of crying cat syndrome due to balanced translocation in one parent].
    Barjaktarović N; Pendić B; Garzicić B; Popovic M; Paljm A
    Nouv Presse Med; 1977 Jan; 6(3):180-2. PubMed ID: 834552
    [TBL] [Abstract][Full Text] [Related]  

  • 33. "Cri-du-chat" syndrome in a patient born to a mother with a paracentric inversion of chromosome 5q.
    Bourthoumieu S; Esclaire F; Terro F; Baclet MC; Bedu A; Dufetelle B; Gilbert B; Barthe D; Yardin C
    Ann Genet; 2003; 46(4):483-6. PubMed ID: 14659787
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Cri-du-chat and trisomy 13 syndromes in an infant with an unbalanced chromosomal translocation.
    Leisti J; Kaback MM; Rimoin DL
    Birth Defects Orig Artic Ser; 1975; 11(5):317-9. PubMed ID: 1218232
    [No Abstract]   [Full Text] [Related]  

  • 35. Amelioration of the typical cognitive phenotype in a patient with the 5pter deletion associated with Cri-du-chat syndrome in addition to a partial duplication of CTNND2.
    Sardina JM; Walters AR; Singh KE; Owen RX; Kimonis VE
    Am J Med Genet A; 2014 Jul; 164A(7):1761-4. PubMed ID: 24677774
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [A case of cri-du-chat syndrome].
    Di Palma L; Iemma R; Di Cesare M; Bottazzi LC
    Minerva Pediatr; 1978 Jan; 30(2):173-8. PubMed ID: 642884
    [No Abstract]   [Full Text] [Related]  

  • 37. Molecular approach to analyzing the human 5p deletion syndrome, cri du chat.
    Carlock LR; Wasmuth JJ
    Somat Cell Mol Genet; 1985 May; 11(3):267-76. PubMed ID: 2988137
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Retinopathy in a Full-Term Infant with Cri-du-Chat Syndrome.
    Chhaya N; Chan T
    R I Med J (2013); 2021 Feb; 104(1):37-39. PubMed ID: 33517598
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Cri-du-chat syndrome: clinical profile and prenatal diagnosis.
    Tullu MS; Muranjan MN; Sharma SV; Sahu DR; Swami SR; Deshmukh CT; Bharucha BA
    J Postgrad Med; 1998; 44(4):101-4. PubMed ID: 10703584
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 12.