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6. Spectrographic analysis of cries from children with maladie du cri du chat. Vuorenkoski V; Lind J; Partanen TJ; Lejeune J; Lafourcade J; Wasz-Höckert O Ann Paediatr Fenn; 1966; 12(3):174-80. PubMed ID: 5964858 [No Abstract] [Full Text] [Related]
7. Cerebellar vermis hypoplasia in a case of cri-du-chat syndrome. De Michele G; Presta M; Di Salle F; Serra L; Mazzaccara A; Della Rocca G; Ambrosio G; Filla A Acta Neurol (Napoli); 1993 Apr; 15(2):92-6. PubMed ID: 8328329 [TBL] [Abstract][Full Text] [Related]
8. [Cri-du-chat syndrome in 2 children]. Goncerzewicz M; Wiśniewski L; Mospinek M; Szymańska J; Krajewska-Walasek M Pediatr Pol; 1980 Jan; 55(1):65-9. PubMed ID: 7367070 [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. 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]
12. 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]
13. [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]
14. [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]
15. 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]
16. [Cri-du-chat syndrome: palmar dermatoglyphics of diagnostic significance]. Benigno V; Cammarata M; Giuffré L Minerva Pediatr; 1985 Mar; 37(5-6):251-3. PubMed ID: 4021951 [No Abstract] [Full Text] [Related]
17. Parental origin of chromosome 5 deletions in the cri-du-chat syndrome. Overhauser J; McMahon J; Oberlender S; Carlin ME; Niebuhr E; Wasmuth JJ; Lee-Chen J Am J Med Genet; 1990 Sep; 37(1):83-6. PubMed ID: 1978567 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Pontine hypoplasia in 5p-syndrome: A key MRI finding for a diagnosis. Ninchoji T; Takanashi J Brain Dev; 2010 Aug; 32(7):571-3. PubMed ID: 19651480 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]