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.
129 related articles for article (PubMed ID: 1004448)
1. [Chromosome abnormalities in a case of Cornelia De Lange syndrome (typus degenerativus amstedolamensis)]. de Angelis P; Ventruto V Minerva Pediatr; 1976 Mar; 28(7):449-53. PubMed ID: 1004448 [No Abstract] [Full Text] [Related]
4. Chromosomal anomaly associated with Cornelia de Lange's syndrome. Szemere G; Godó B; Osváth P; Lehrner J; Pataki O Acta Paediatr Acad Sci Hung; 1972; 13(1):51-5. PubMed ID: 4652495 [No Abstract] [Full Text] [Related]
5. [Chromosome anomalies in a case of Cornelia De Lange syndrome]. Accorsi A Minerva Pediatr; 1971 Jun; 23(25):1105-6. PubMed ID: 5559675 [No Abstract] [Full Text] [Related]
6. NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome. Borck G; Redon R; Sanlaville D; Rio M; Prieur M; Lyonnet S; Vekemans M; Carter NP; Munnich A; Colleaux L; Cormier-Daire V J Med Genet; 2004 Dec; 41(12):e128. PubMed ID: 15591270 [No Abstract] [Full Text] [Related]
7. A de novo t (X;8)(p11.2;q24.3) demonstrating Cornelia de Lange syndrome phenotype. Egemen A; Ulger Z; Ozkinay F; Gulen F; Cogulu O Genet Couns; 2005; 16(1):27-30. PubMed ID: 15844775 [TBL] [Abstract][Full Text] [Related]
8. [4 cases of Cornelia De Lange syndrome (tipus degenerativus Amstelodamensis)]. Calò S; Radice C; Conconi G Riv Clin Pediatr; 1968; 81(4):388-97. PubMed ID: 5761106 [No Abstract] [Full Text] [Related]
10. [Typus degenerativus amstelodamensis. The Cornelia de Lange syndrome in 2 children]. Seemanová E; Losan F; Salichová J Cas Lek Cesk; 1979 Mar; 118(13):404-7. PubMed ID: 455352 [No Abstract] [Full Text] [Related]
11. ["Status degenerativus amstelodamensis"; case report with study of the karyotype]. Crisalli M; Castellani R; Monteverde R Pediatria (Napoli); 1967; 75(4):610-8. PubMed ID: 5586718 [No Abstract] [Full Text] [Related]
12. [Cornelia De Lange syndrome. Clinical contribution of 2 cases]. Li Moli S Riv Clin Pediatr; 1968; 81(4):361-7. PubMed ID: 5759711 [No Abstract] [Full Text] [Related]
13. The Cornelia de Lange syndrome in Singapore. Boon WH J Singapore Paediatr Soc; 1969 Apr; 11(1):25-37. PubMed ID: 5366336 [No Abstract] [Full Text] [Related]
15. [Brachmann-de Lange syndrome in 16 of our patients]. Pankau R; Johannson W; Meinecke P Monatsschr Kinderheilkd; 1990 Feb; 138(2):72-6. PubMed ID: 2320015 [TBL] [Abstract][Full Text] [Related]
16. [Autopsy case of Cornelia de Lange syndrome with chromosome abnormalities]. Kubota Y; Okada Y; Matsui I; Hayashi Y; Takazawa H Nihon Shonika Gakkai Zasshi; 1970 Jan; 74(1):1-9. PubMed ID: 5462021 [No Abstract] [Full Text] [Related]
17. Chromosome 13q deletion with Cornelia de Lange syndrome phenotype. Ngo CT; Alhady M; Tan AK; Norlasiah IS; Ong GB; Chua CN Med J Malaysia; 2007 Mar; 62(1):74-5. PubMed ID: 17682579 [TBL] [Abstract][Full Text] [Related]
18. A Malay boy with the Cornelia de Lange syndrome: clinical and molecular findings. Bhuiyan ZA; Zilfalil BA; Hennekam RC Singapore Med J; 2006 Aug; 47(8):724-7. PubMed ID: 16865217 [TBL] [Abstract][Full Text] [Related]
19. [On the Cornelia De Lange syndrome. (Clinical contribution)]. Normale M; Pinta-Boccalatte MF; Castaldo A Pediatria (Napoli); 1972; 80(4):368-87. PubMed ID: 4646631 [No Abstract] [Full Text] [Related]
20. [Typus degenerativus amstelodamensis (Cornelia de Lange disease). Case reports]. Mignone F; Ravetto F Minerva Pediatr; 1966 Feb; 18(6):291-9. PubMed ID: 5930941 [No Abstract] [Full Text] [Related] [Next] [New Search]