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 *

122 related articles for article (PubMed ID: 31187941)

  • 21. The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features.
    Niebuhr E
    Hum Genet; 1978 Nov; 44(3):227-75. PubMed ID: 365706
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Psychomotor Development in Cri du Chat Syndrome: Comparison in Two Italian Cohorts with Different Rehabilitation Methods.
    Guala A; Spunton M; Tognon F; Pedrinazzi M; Medolago L; Cerutti Mainardi P; Spairani S; Malacarne M; Finale E; Comelli M; Danesino C
    ScientificWorldJournal; 2016; 2016():3125283. PubMed ID: 28004033
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cri du chat syndrome due to meiotic recombination in a pericentric inversion 5 carrier.
    Chernos JE; Fowlow SB; Cox DM
    Clin Genet; 1992 May; 41(5):266-9. PubMed ID: 1606717
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [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]  

  • 25. Prevalence of autism spectrum phenomenology in Cornelia de Lange and Cri du Chat syndromes.
    Moss JF; Oliver C; Berg K; Kaur G; Jephcott L; Cornish K
    Am J Ment Retard; 2008 Jul; 113(4):278-91. PubMed ID: 18564888
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal diagnosis of cri du chat (5p-) syndrome in association with isolated moderate bilateral ventriculomegaly.
    Stefanou EG; Hanna G; Foakes A; Crocker M; Fitchett M
    Prenat Diagn; 2002 Jan; 22(1):64-6. PubMed ID: 11810654
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. 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]  

  • 30. Cri du chat syndrome determined by the 5p15.3-->pter deletion--diagnostic problems.
    Laczmanska I; Stembalska A; Gil J; Czemarmazowicz H; Sasiadek M
    Eur J Med Genet; 2006; 49(1):87-92. PubMed ID: 16473315
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Growth charts for cri-du-chat syndrome: an international collaborative study.
    Marinescu RC; Mainardi PC; Collins MR; Kouahou M; Coucourde G; Pastore G; Eaton-Evans J; Overhauser J
    Am J Med Genet; 2000 Sep; 94(2):153-62. PubMed ID: 10982972
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Cri-Du-Chat Syndrome: Clinical Profile and Chromosomal Microarray Analysis in Six Patients.
    Espirito Santo LD; Moreira LM; Riegel M
    Biomed Res Int; 2016; 2016():5467083. PubMed ID: 27144168
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Social Economic Costs, Health-Related Quality of Life and Disability in Patients with Cri Du Chat Syndrome.
    Kodra Y; Cavazza M; de Santis M; Guala A; Liverani ME; Armeni P; Masini M; Taruscio D
    Int J Environ Res Public Health; 2020 Aug; 17(16):. PubMed ID: 32824402
    [No Abstract]   [Full Text] [Related]  

  • 35. Goldenhar and cri-du-chat syndromes: a contiguous gene deletion syndrome?
    Choong YF; Watts P; Little E; Beck L
    J AAPOS; 2003 Jun; 7(3):226-7. PubMed ID: 12825068
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [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]  

  • 37. Marfan and cri du chat syndromes in an 18-month-old child: evidence of phenotype interaction.
    McClellan MW; Golden WL; Wilson WG
    Clin Genet; 1994 Oct; 46(4):319-21. PubMed ID: 7834900
    [TBL] [Abstract][Full Text] [Related]  

  • 38. del5p/dup5q in a 'cri du chat' patient without parental chromosomal rearrangement.
    Akalin I; Yararbas K; Akgul N; Babaoglu E; Akay GG; Dyer S; Kutlay NY; Ruhi HI; Kog G; Tukun A
    Am J Med Genet A; 2006 May; 140(9):1016-20. PubMed ID: 16619202
    [No Abstract]   [Full Text] [Related]  

  • 39. [Accidental finding of a cri du chat syndrome in an adult patient by means of array-CGH].
    Ferreirós-Martínez R; López-Manzanares L; Alonso-Cerezo C
    Rev Neurol; 2014 Jul; 59(2):71-6. PubMed ID: 25005318
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Sleep in individuals with Cri du Chat syndrome: a comparative study.
    Maas AP; Didden R; Korzilius H; Braam W; Smits MG; Curfs LM
    J Intellect Disabil Res; 2009 Aug; 53(8):704-15. PubMed ID: 19508289
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.