322 related articles for article (PubMed ID: 15849798)
1. Dandy-Walker syndrome and corpus callosum agenesis in 5p deletion.
Vialard F; Robyr R; Hillion Y; Molina Gomes D; Selva J; Ville Y
Prenat Diagn; 2005 Apr; 25(4):311-3. PubMed ID: 15849798
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Prenatal diagnosis of 5p deletion syndrome following abnormally low maternal serum human chorionic gonadotrophin.
Weiss A; Shalev S; Weiner E; Shneor Y; Shalev E
Prenat Diagn; 2003 Jul; 23(7):572-4. PubMed ID: 12868086
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Cytogenetic and molecular characterization of a three-generation family with chromosome 5p terminal deletion.
Fang JS; Lee KF; Huang CT; Syu CL; Yang KJ; Wang LH; Liao DL; Chen CH
Clin Genet; 2008 Jun; 73(6):585-90. PubMed ID: 18400035
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [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]
9. Association of severe autosomal recessive osteopetrosis and Dandy-Walker syndrome with agenesis of the corpus callosum.
Ben Hamouda H; Sfar MN; Braham R; Ben Salah M; Ayadi A; Soua H; Hamza H; Sfar MT
Acta Orthop Belg; 2001 Dec; 67(5):528-32. PubMed ID: 11822087
[TBL] [Abstract][Full Text] [Related]
10. Agenesis of the corpus callosum and Dandy-Walker malformation associated with hemimegalencephaly in the sebaceous nevus syndrome.
Dodge NN; Dobyns WB
Am J Med Genet; 1995 Mar; 56(2):147-50. PubMed ID: 7625436
[TBL] [Abstract][Full Text] [Related]
11. A yeast artificial chromosome contig of the critical region for cri-du-chat syndrome.
Goodart SA; Simmons AD; Grady D; Rojas K; Moyzis RK; Lovett M; Overhauser J
Genomics; 1994 Nov; 24(1):63-8. PubMed ID: 7896290
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. 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]
16. 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]
17. Prenatal diagnosis of minute 5p- deletion: a cytogenetic problem in detection.
Benn PA; Hsu LY; Verma RS; Alonso ML; Reich E; Wishnick M
Obstet Gynecol; 1987 Sep; 70(3 Pt 2):449-52. PubMed ID: 3627600
[TBL] [Abstract][Full Text] [Related]
18. [Dissection and cytogenetic localization of the phenotypes of the 5p deletion syndrome].
Dan M; Niebuhr A; Zhang X; Zhang X; Gao C
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1998 Oct; 20(5):339-44. PubMed ID: 11717989
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Clinical delineation of a patient with trisomy 1q32.qter and monosomy 5p resulting from a familial translocation 1;5.
Flores Ramírez F; Abreu González M; García Delgado C; Aparicio Onofre A; Guevara Yáñez R; Sánchez Urbina R; Murguía Peniche T; Ramírez-Ortíz MA; Ibarra Ríos D; Ortiz de Luna RI; Cervantes Peredo AB; Morán Barroso VF
Genet Couns; 2010; 21(4):363-73. PubMed ID: 21290965
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
