292 related articles for article (PubMed ID: 25236835)
21. 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]
22. 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]
23. 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]
24. 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]
25. Fertility and the cri du chat syndrome.
Martínez JE; Tuck-Muller CM; Superneau D; Wertelecki W
Clin Genet; 1993 Apr; 43(4):212-4. PubMed ID: 8330455
[TBL] [Abstract][Full Text] [Related]
26. Development of diagnostic tools for the analysis of 5p deletions using interphase FISH.
Gersh M; Grady D; Rojas K; Lovett M; Moyzis R; Overhauser J
Cytogenet Cell Genet; 1997; 77(3-4):246-51. PubMed ID: 9284926
[TBL] [Abstract][Full Text] [Related]
27. [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]
28. [Cri-du-chat syndrome--a case report].
Chiu CP; Lin TY
Changgeng Yi Xue Za Zhi; 1986 Jun; 9(2):134-8. PubMed ID: 3454700
[No Abstract] [Full Text] [Related]
29. [Prognosis in the cri-du-chat syndrome].
Oosterwijk JC; Verboom AJ; Bijlsma JB
Tijdschr Kindergeneeskd; 1987 Dec; 55(6):226-33. PubMed ID: 3327195
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. [Cytogenetic and molecular genetic diagnosis of a neonate with partial 13q trisomy and partial 5p monosomy].
Xiao W; Gao Z; Meng Q; Zhang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):747-9. PubMed ID: 25449080
[TBL] [Abstract][Full Text] [Related]
32. Cri du chat and Turner syndrome features in a newborn girl with an unbalanced 45,X,psu dic(5;X)(p15.2;p22.1) karyotype: FISH and replication banding studies.
Reddy KS; Smith DL; Ball CS
Ann Genet; 1999; 42(2):105-8. PubMed ID: 10434125
[TBL] [Abstract][Full Text] [Related]
33. Cri du chat syndrome patients have DNA methylation changes in genes linked to symptoms of the disease.
Holland P; Wildhagen M; Istre M; Reiakvam OM; Dahl JA; Søraas A
Clin Epigenetics; 2022 Oct; 14(1):128. PubMed ID: 36242045
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. 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]
36. [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]
37. A de novo chromosomal abnormality in Cri du Chat syndrome.
Sun SC; Luo FW; Zhou ZM; Peng YS; Song HW
Indian J Pediatr; 2014 Jul; 81(7):722-5. PubMed ID: 23900752
[TBL] [Abstract][Full Text] [Related]
38. Two cases of deletion 5p syndrome: one with paternal involvement and another with atypical presentation.
Azman BZ; Akhir SM; Zilfalil BA; Ankathil R
Singapore Med J; 2008 Apr; 49(4):e98-e100. PubMed ID: 18418516
[TBL] [Abstract][Full Text] [Related]
39. Cri du chat syndrome and primary ciliary dyskinesia: a common genetic cause on chromosome 5p.
Shapiro AJ; Weck KE; Chao KC; Rosenfeld M; Nygren AO; Knowles MR; Leigh MW; Zariwala MA
J Pediatr; 2014 Oct; 165(4):858-61. PubMed ID: 25066065
[TBL] [Abstract][Full Text] [Related]
40. Large distal 5p deletion with hemifacial microsomia and absence of cri-du-chat syndrome.
Wang JC; Khan A
Clin Dysmorphol; 2010 Jan; 19(1):38-39. PubMed ID: 19923986
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
