References analysis of the Wikipedia article "Cornelia de Lange syndrome" in the English version

doi.org

Kline, Antonie D.; Moss, Joanna F.; Selicorni, Angelo; Bisgaard, Anne-Marie; Deardorff, Matthew A.; Gillett, Peter M.; Ishman, Stacey L.; Kerr, Lynne M.; Levin, Alex V.; Mulder, Paul A.; Ramos, Feliciano J.; Wierzba, Jolanta; Ajmone, Paola Francesca; Axtell, David; Blagowidow, Natalie; Cereda, Anna; Costantino, Antonella; Cormier-Daire, Valerie; FitzPatrick, David; Grados, Marco; Groves, Laura; Guthrie, Whitney; Huisman, Sylvia; Kaiser, Frank J.; Koekkoek, Gerritjan; Levis, Mary; Mariani, Milena; McCleery, Joseph P.; Menke, Leonie A.; Metrena, Amy; O'Connor, Julia; Oliver, Chris; Pie, Juan; Piening, Sigrid; Potter, Carol J.; Quaglio, Ana L.; Redeker, Egbert; Richman, David; Rigamonti, Claudia; Shi, Angell; Tümer, Zeynep; Van Balkom, Ingrid D. C.; Hennekam, Raoul C. (October 2018). "Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement". Nature Reviews Genetics. 19 (10): 649–666. doi:10.1038/s41576-018-0031-0. PMC 7136165. PMID 29995837.

Basel-Vanagaite, L.; Wolf, L.; Orin, M.; Larizza, L.; Gervasini, C.; Krantz, I.D.; Deardoff, M.A. (2016). "Recognition of the Cornelia de Lange syndrome phenotype with facial dysmorphology novel analysis". Clinical Genetics. 89 (5): 557–563. doi:10.1111/cge.12716. PMID 26663098. S2CID 45748040.

Kline AD, Grados M, Sponseller P, Levy HP, Blagowidow N, Schoedel C, Rampolla J, Clemens DK, Krantz I, Kimball A, Pichard C, Tuchman D (2007). "Natural history of aging in Cornelia de Lange syndrome". Am J Med Genet C Semin Med Genet. 145C (3): 248–60. doi:10.1002/ajmg.c.30137. PMC 4902018. PMID 17640042.

Liu, J; Krantz, ID (October 2009). "Cornelia de Lange syndrome, cohesin, and beyond". Clinical Genetics. 76 (4): 303–314. doi:10.1111/j.1399-0004.2009.01271.x. PMC 2853897. PMID 19793304.

Panarotto, Melanie (April 2022). "Cornelia de Lange syndrome mutations in NIPBL can impair cohesin-mediated DNA loop extrusion". PNAS. 119 (18): e2201029119. Bibcode:2022PNAS..11901029P. doi:10.1073/pnas.2201029119. PMC 9170158. PMID 35476527.https://www.pnas.org/doi/full/10.1073/pnas.2201029119

Krantz, Ian D; McCallum, Jennifer; DeScipio, Cheryl; Kaur, Maninder; Gillis, Lynette A; Yaeger, Dinah; Jukofsky, Lori; Wasserman, Nora; Bottani, Armand; Morris, Colleen A; Nowaczyk, Malgorzata J M; Toriello, Helga; Bamshad, Michael J; Carey, John C; Rappaport, Eric; Kawauchi, Shimako; Lander, Arthur D; Calof, Anne L; Li, Hui-hua; Devoto, Marcella; Jackson, Laird G (June 2004). "Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B". Nature Genetics. 36 (6): 631–635. doi:10.1038/ng1364. PMC 4902017. PMID 15146186.

Tonkin E, Wang TJ, Lisgo S, Bamshad MJ, Strachan T (2004). "NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome". Nature Genetics. 36 (6): 636–641. doi:10.1038/ng1363. PMID 15146185.

Krantz, Ian D.; Tonkin, Emma; Smith, Melanie; Devoto, Marcella; Bottani, Armand; Simpson, Claire; Hofreiter, Mary; Abraham, Vinod; Jukofsky, Lori; Conti, Brian P.; Strachan, Tom; Jackson, Laird (2001). "Exclusion of linkage to the CDL1 gene region on chromosome 3q26.3 in some familial cases of Cornelia de Lange syndrome". American Journal of Medical Genetics. 101 (2): 120–129. doi:10.1002/1096-8628(20010615)101:2<120::AID-AJMG1319>3.0.CO;2-G. PMC 4896160. PMID 11391654.

Kaur, Maninder; Blair, Justin; Devkota, Batsal; Fortunato, Sierra; Clark, Dinah; Lawrence, Audrey; Kim, Jiwoo; Do, Wonwook; Semeo, Benjamin; Katz, Olivia; Mehta, Devanshi; Yamamoto, Nobuko; Schindler, Emma; Al Rawi, Zayd; Wallace, Nina (August 2023). "Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms". American Journal of Medical Genetics Part A. 191 (8): 2113–2131. doi:10.1002/ajmg.a.63247. ISSN 1552-4825. PMC 10524367. PMID 37377026.

Boyle, M.I.; Jespersgaard, C.; Brøndum-Nielsen, K.; Bisgaard, A.-M.; Tümer, Z. (July 2015). "Cornelia de Lange syndrome". Clinical Genetics. 88 (1): 1–12. doi:10.1111/cge.12499. PMID 25209348. S2CID 37580405.

Pié, Juan; Gil-Rodríguez, María Concepción; Ciero, Milagros; López-Viñas, Eduardo; Ribate, María Pilar; Arnedo, María; Deardorff, Matthew A.; Puisac, Beatriz; Legarreta, Jesús; de Karam, Juan Carlos; Rubio, Encarnación; Bueno, Inés; Baldellou, Antonio; Calvo, Mª Teresa; Casals, Nuria; Olivares, José Luis; Losada, Ana; Hegardt, Fausto G.; Krantz, Ian D.; Gómez-Puertas, Paulino; Ramos, Feliciano J. (April 2010). "Mutations and variants in the cohesion factor genes NIPBL , SMC1A , and SMC3 in a cohort of 30 unrelated patients with Cornelia de Lange syndrome". American Journal of Medical Genetics Part A. 152A (4): 924–929. doi:10.1002/ajmg.a.33348. PMC 2923429. PMID 20358602.

Wiesmann, U. N.; DiDonato, S.; Herschkowitz, N. N. (1975-10-27). "Effect of chloroquine on cultured fibroblasts: release of lysosomal hydrolases and inhibition of their uptake". Biochemical and Biophysical Research Communications. 66 (4): 1338–1343. doi:10.1016/0006-291x(75)90506-9. ISSN 1090-2104. PMID 4.

Middelhoven., Ada (November 1950). "Professor Cornelia de Lange in Memoriam". Acta Paediatrica. 39 (1): 177–178. doi:10.1111/j.1651-2227.1950.tb08518.x. ISSN 0803-5253. PMID 15432173.

Friedel, Georges (1933). "Sur un nouveau type de macles". Bulletin de la Société française de Minéralogie. 56 (4): 262–274. doi:10.3406/bulmi.1933.4170. ISSN 0366-3248.

Opitz, John M.; Reynolds, James F. (September 1985). "The Brachmann-de Lange syndrome". American Journal of Medical Genetics. 22 (1): 89–102. doi:10.1002/ajmg.1320220110. ISSN 0148-7299. PMID 3901753.

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Liu, J; Krantz, ID (October 2009). "Cornelia de Lange syndrome, cohesin, and beyond". Clinical Genetics. 76 (4): 303–314. doi:10.1111/j.1399-0004.2009.01271.x. PMC 2853897. PMID 19793304.

Middelhoven., Ada (November 1950). "Professor Cornelia de Lange in Memoriam". Acta Paediatrica. 39 (1): 177–178. doi:10.1111/j.1651-2227.1950.tb08518.x. ISSN 0803-5253. PMID 15432173.

ncbi.nlm.nih.gov

Liu, J; Krantz, ID (October 2009). "Cornelia de Lange syndrome, cohesin, and beyond". Clinical Genetics. 76 (4): 303–314. doi:10.1111/j.1399-0004.2009.01271.x. PMC 2853897. PMID 19793304.

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