134 related articles for article (PubMed ID: 10982972)
1. Growth charts for cri-du-chat syndrome: an international collaborative study.
Marinescu RC; Mainardi PC; Collins MR; Kouahou M; Coucourde G; Pastore G; Eaton-Evans J; Overhauser J
Am J Med Genet; 2000 Sep; 94(2):153-62. PubMed ID: 10982972
[TBL] [Abstract][Full Text] [Related]
2. Growth study of cri du chat syndrome.
Collins MS; Eaton-Evans J
Arch Dis Child; 2001 Oct; 85(4):337-8. PubMed ID: 11567947
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Fertility and the cri du chat syndrome.
MartÃnez JE; Tuck-Muller CM; Superneau D; Wertelecki W
Clin Genet; 1993 Apr; 43(4):212-4. PubMed ID: 8330455
[TBL] [Abstract][Full Text] [Related]
6. Studies of the cranial base in 23 patients with cri-du-chat syndrome suggest a cranial developmental field involved in the condition.
Kjaer I; Niebuhr E
Am J Med Genet; 1999 Jan; 82(1):6-14. PubMed ID: 9916835
[TBL] [Abstract][Full Text] [Related]
7. Marfan and cri du chat syndromes in an 18-month-old child: evidence of phenotype interaction.
McClellan MW; Golden WL; Wilson WG
Clin Genet; 1994 Oct; 46(4):319-21. PubMed ID: 7834900
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Anthropometry in the Cri du Chat syndrome.
Niebuhr E
Clin Genet; 1979 Aug; 16(2):82-95. PubMed ID: 477023
[TBL] [Abstract][Full Text] [Related]
11. Anesthesia in Cri du Chat syndrome: Information on 51 Italian patients.
Guala A; Spunton M; Mainardi PC; Emmig U; Acucella G; Danesino C
Am J Med Genet A; 2015 May; 167A(5):1168-70. PubMed ID: 25820652
[No Abstract] [Full Text] [Related]
12. Goldenhar and cri-du-chat syndromes: a contiguous gene deletion syndrome?
Choong YF; Watts P; Little E; Beck L
J AAPOS; 2003 Jun; 7(3):226-7. PubMed ID: 12825068
[TBL] [Abstract][Full Text] [Related]
13. Measurements on hand radiographs from 32 cri-du-chat probands.
Fenger K; Niebuhr E
Radiology; 1978 Oct; 129(1):137-41. PubMed ID: 693865
[TBL] [Abstract][Full Text] [Related]
14. Protein-energy malnutrition is frequent and precocious in children with cri du chat syndrome.
Lefranc V; de Luca A; Hankard R
Am J Med Genet A; 2016 May; 170A(5):1358-62. PubMed ID: 26872355
[TBL] [Abstract][Full Text] [Related]
15. Skin picking disorder in 97 Italian and Spanish Cri du chat patients.
Spunton M; Guala A; Liverani ME; Medolago L; Tognon F; Casado F; Del Valle M; Porras J; Larrea I; Porta G; Albani G; Nevado J; Danesino C
Am J Med Genet A; 2019 Aug; 179(8):1525-1530. PubMed ID: 31187941
[TBL] [Abstract][Full Text] [Related]
16. [A de novo partial 5p deletion and cryptic 18p duplication detected by SNP-Array in a boy featuring Cri du Chat syndrome].
Hu JC; Tan K; Cheng DH; Li LY; Lu GX; Tan YQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):87-90. PubMed ID: 23450488
[TBL] [Abstract][Full Text] [Related]
17. Cri du chat syndrome: changing phenotype in older patients.
Van Buggenhout GJ; Pijkels E; Holvoet M; Schaap C; Hamel BC; Fryns JP
Am J Med Genet; 2000 Jan; 90(3):203-15. PubMed ID: 10678657
[TBL] [Abstract][Full Text] [Related]
18. Phenotypic and phoniatric findings in mosaic cri du chat syndrome.
Romano C; Ragusa RM; Scillato F; Greco D; Amato G; Barletta C
Am J Med Genet; 1991 Jun; 39(4):391-5. PubMed ID: 1877615
[TBL] [Abstract][Full Text] [Related]
19. The "cri du chat" syndrome.
Mladkovskaya TB; Lebedev BV; Mazaeva IV
Sov Genet; 1970 Oct; 6(10):1374-9. PubMed ID: 4272596
[No Abstract] [Full Text] [Related]
20. Unusual ocular findings in an infant with cri-du-chat syndrome.
Kitsiou-Tzeli S; Dellagrammaticas HD; Papas CB; Ladas ID; Bartsocas CS
J Med Genet; 1983 Aug; 20(4):304-7. PubMed ID: 6620332
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]