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 *

105 related articles for article (PubMed ID: 292652)

  • 1. Orofacial manifestations in the Cri du Chat syndrome (5p-).
    Scully C; Davison MF
    J Dent; 1979 Dec; 7(4):313-20. PubMed ID: 292652
    [No Abstract]   [Full Text] [Related]  

  • 2. "Cri du chat" syndrome with maternal insertional translocation.
    Berger R; Touati G; Derre J; Ortiz MA; Martinetti J
    Clin Genet; 1974; 5(5):428-32. PubMed ID: 4368036
    [No Abstract]   [Full Text] [Related]  

  • 3. A systematic review of the oral and craniofacial manifestations of cri du chat syndrome.
    Corcuera-Flores JR; Casttellanos-Cosano L; Torres-Lagares D; Serrera-Figallo MÁ; Rodríguez-Caballero Á; Machuca-Portillo G
    Clin Anat; 2016 Jul; 29(5):555-60. PubMed ID: 26457586
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Assessment of orofacial characteristics and oral pathology associated with cri-du-chat syndrome.
    Rodríguez-Caballero A; Torres-Lagares D; Yáñez-Vico RM; Gutiérrez-Pérez JL; Machuca-Portillo G
    Oral Dis; 2012 Mar; 18(2):191-7. PubMed ID: 22035137
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. The orofacial structures and their association with congenital abnormalities.
    Stewart RE; Poole AE
    Pediatr Clin North Am; 1982 Jun; 29(3):547-84. PubMed ID: 7045798
    [No Abstract]   [Full Text] [Related]  

  • 7. Cri du chat syndrome and translocation t(5p--;18p+).
    Abrisqueta JA; Perez A; Aller V; Del Mazo J; Goday C; Martin MA; De Torres ML
    J Genet Hum; 1976 Sep; 24(3):173-82. PubMed ID: 1003171
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Rare developmental anomalies in children: 1) the cri du chat syndrome, karyotype: 46, XY, DEL (5) (P31); 2) the mixed type of syndrome with signs of Patau's syndrome and the cri du chat syndrome, karyotype: 46, XY, DER (5) T (5, 13) (P14, Q14) MAT].
    Badalian LO; Malygina NA; Mutovin GR; Petrukhin AS; Nikonov VP
    Pediatriia; 1980 Mar; (3):74-7. PubMed ID: 7375280
    [No Abstract]   [Full Text] [Related]  

  • 9. Hemifacial microsomia in cri du chat (5p-) syndrome.
    Neu KW; Friedman JM; Howard-Peebles PN
    J Craniofac Genet Dev Biol; 1982; 2(4):295-8. PubMed ID: 7183708
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. The cri du chat syndrome: neuropathologic observations.
    Solitare GB
    J Ment Defic Res; 1967 Dec; 11(4):267-77. PubMed ID: 5582929
    [No 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. The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-).
    Breg WR; Steele MW; Miller OJ; Warburton D; DeCapoa A; Allderdice PW
    J Pediatr; 1970 Nov; 77(5):782-91. PubMed ID: 5504069
    [No Abstract]   [Full Text] [Related]  

  • 14. A three-generation family with terminal microdeletion involving 5p15.33-32 due to a whole-arm 5;15 chromosomal translocation with a steady phenotype of atypical cri du chat syndrome.
    Elmakky A; Carli D; Lugli L; Torelli P; Guidi B; Falcinelli C; Fini S; Ferrari F; Percesepe A
    Eur J Med Genet; 2014 Mar; 57(4):145-50. PubMed ID: 24556499
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial monosomy 22 as the result of an unbalanced translocation 5:22 in a patient with cri-du-chat syndrome.
    Silengo MC; Andria G
    Hum Genet; 1976 Dec; 34(3):319-22. PubMed ID: 1002156
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Two cases of cri-du-chat syndrome with mild phenotypic effect but with different size of 5p deletion.
    Smith A; Field B; Murray R; Nelson J
    J Paediatr Child Health; 1990 Jun; 26(3):152-4. PubMed ID: 2206616
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mosaic Cri du Chat syndrome in a patient exhibiting three 5p cell lines.
    Kitsiou S; Kolialexi A; Mavrou A
    Prenat Diagn; 2004 Jul; 24(7):578-9. PubMed ID: 15300755
    [No Abstract]   [Full Text] [Related]  

  • 18. [An autopsy case of cri du chat syndrome: The fifth case report of ring chromosome].
    Chuang SM; Chen SH; Yang CP
    Taiwan Yi Xue Hui Za Zhi; 1976 May; 75(5):282-9. PubMed ID: 1066440
    [No Abstract]   [Full Text] [Related]  

  • 19. Cri-du-chat syndrome in a child with a 5/15 translocation and interstitial centromeric heterochromatin.
    Gebauer HJ; Stumpf B; Hansmann I; Grimm T
    Clin Genet; 1978 Dec; 14(6):345-50. PubMed ID: 83210
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cri du chat syndrome [46, XY, 5p-] with balanced B/F translocation in father and grandfather: a case report.
    Char F
    Birth Defects Orig Artic Ser; 1974; 10(10):49-53. PubMed ID: 4462641
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.