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.
2. Wolf-Hirschhorn and Cri du Chat syndromes resulting from familial translocations: 3 further examples of the Bp monosomy epistatic effect. Petit P; Fryns JP Genet Couns; 1990; 1(2):179-84. PubMed ID: 2081002 [TBL] [Abstract][Full Text] [Related]
3. Determination of the 'critical region' for cat-like cry of Cri-du-chat syndrome and analysis of candidate genes by quantitative PCR. Wu Q; Niebuhr E; Yang H; Hansen L Eur J Hum Genet; 2005 Apr; 13(4):475-85. PubMed ID: 15657623 [TBL] [Abstract][Full Text] [Related]
4. 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]
6. 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]
7. The larynx in the cri du chat (cat cry) syndrome. Ward PH; Engel E; Nance WE Laryngoscope; 1968 Oct; 78(10):1716-33. PubMed ID: 5681688 [No Abstract] [Full Text] [Related]
8. 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]
10. [Cri-du-chat syndrome. A case report]. Diop IB; Sy Signate H; Ba SA; Sarr M; Hane L; Diame H; Kane A; Dieye O; Sow D; Diouf SM; Fall M Dakar Med; 2000; 45(1):95-7. PubMed ID: 14666800 [TBL] [Abstract][Full Text] [Related]
12. [Additional data on the pathogenesis of the crying cat syndrome]. Gajewska-Obel E; Kowalczyk J; Modzelewska I Pediatr Pol; 1986 May; 61(5):305-7. PubMed ID: 3786022 [No Abstract] [Full Text] [Related]
13. Ocular findings in a newborn with cri du chat syndrome. Schechter RJ Ann Ophthalmol; 1978 Mar; 10(3):339-44. PubMed ID: 418724 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. The larynx in the cri du chat (cat cry) syndrome. Ward PH; Engel E; Nance WE Trans Am Acad Ophthalmol Otolaryngol; 1968; 72(1):90-102. PubMed ID: 5637525 [No Abstract] [Full Text] [Related]
18. [Partial B trisomy in cat-cry-syndrome (author's transl)]. Schwingshackl A; Ganner E Padiatr Padol; 1973; 8(4):362-71. PubMed ID: 4745566 [No Abstract] [Full Text] [Related]
19. 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]
20. [A case of deletion of the short arm of chromosome 5 in Vietnam (crying cat syndrome)]. Lichtenberger M; Morineaud JP Ann Pediatr (Paris); 1967 Mar; 14(3):234-47. PubMed ID: 5614548 [No Abstract] [Full Text] [Related] [Next] [New Search]