158 related articles for article (PubMed ID: 25136230)
21. Brachman de Lange syndrome.
Verma L; Passi S; Gauba K
Contemp Clin Dent; 2010 Oct; 1(4):268-70. PubMed ID: 22114436
[TBL] [Abstract][Full Text] [Related]
22. Severe ipsilateral musculoskeletal involvement in a Cornelia de Lange patient with a novel NIPBL mutation.
Baquero-Montoya C; Gil-Rodríguez MC; Hernández-Marcos M; Teresa-Rodrigo ME; Vicente-Gabas A; Bernal ML; Casale CH; Bueno-Lozano G; Bueno-Martínez I; Queralt E; Villa O; Hernando-Davalillo C; Armengol L; Gómez-Puertas P; Puisac B; Selicorni A; Ramos FJ; Pié J
Eur J Med Genet; 2014 Sep; 57(9):503-9. PubMed ID: 24874887
[TBL] [Abstract][Full Text] [Related]
23. [Cornelia de Lange Syndrome and multiple hormonal deficiency, an unusual association. Clinical case].
Mora-Bautista VM; Mendoza-Rojas V; Contreras-García GA
Arch Argent Pediatr; 2017 Jun; 115(3):e170-e174. PubMed ID: 28504504
[TBL] [Abstract][Full Text] [Related]
24. Ultrasonographic and clinical appearance of a 22-week-old fetus with Brachmann-de Lange syndrome.
Urban M; Hartung J
Am J Med Genet; 2001 Jul; 102(1):73-5. PubMed ID: 11471176
[TBL] [Abstract][Full Text] [Related]
25. Identification of a novel de novo mutation in the NIPBL gene in an Iranian patient with Cornelia de Lange syndrome: A case report.
Galehdari H; Monajemzadeh R; Nazem H; Mohamadian G; Pedram M
J Med Case Rep; 2011 Jun; 5():242. PubMed ID: 21707975
[TBL] [Abstract][Full Text] [Related]
26. Wiedemann-Steiner Syndrome as a Differential Diagnosis of Cornelia de Lange Syndrome Using Targeted Next-Generation Sequencing: A Case Report.
Demir S; Gürkan H; Öz V; Yalçıntepe S; Atlı EI; Atlı E
Mol Syndromol; 2021 Mar; 12(1):46-51. PubMed ID: 33776627
[TBL] [Abstract][Full Text] [Related]
27. Clinical and genetic analysis of Korean patients with Cornelia de Lange syndrome: two novel NIPBL mutations.
Park HD; Ki CS; Kim JW; Kim WT; Kim JK
Ann Clin Lab Sci; 2010; 40(1):20-5. PubMed ID: 20124326
[TBL] [Abstract][Full Text] [Related]
28. [Cornelia de Lange syndrome: report of a case and the review of literature on 17 cases].
Hei MY; Chen J; Wu LQ; Yu B; Tan YJ; Zhao LL
Zhonghua Er Ke Za Zhi; 2012 Aug; 50(8):606-11. PubMed ID: 23158739
[TBL] [Abstract][Full Text] [Related]
29. A newborn with Cornelia de Lange syndrome: a case report.
Uzun H; Senses DA; Uluba M; Kocabay K
Cases J; 2008 Nov; 1(1):329. PubMed ID: 19019222
[TBL] [Abstract][Full Text] [Related]
30. [A case of Cornelia de Lange syndrome with retentio testis].
Satomi S; Terada T; Katayama T
Hinyokika Kiyo; 1985 Jul; 31(7):1203-10. PubMed ID: 2865886
[TBL] [Abstract][Full Text] [Related]
31. A Korean case of Cornelia de Lange syndrome.
Kim IT; Park JW; Choi WC
Korean J Ophthalmol; 2005 Jun; 19(2):153-5. PubMed ID: 15988935
[TBL] [Abstract][Full Text] [Related]
32. Clinical Diagnosis of Classical Cornelia de Lange Syndrome Made From Postmortem Examination of Second Trimester Fetus With Novel
Hague J; Twiss P; Mead Z; Park SM
Pediatr Dev Pathol; 2019 Oct; 22(5):475-479. PubMed ID: 30890023
[TBL] [Abstract][Full Text] [Related]
33. Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience.
Bhuiyan ZA; Klein M; Hammond P; van Haeringen A; Mannens MM; Van Berckelaer-Onnes I; Hennekam RC
J Med Genet; 2006 Jul; 43(7):568-75. PubMed ID: 16236812
[TBL] [Abstract][Full Text] [Related]
34. Cornelia de Lange syndrome: a case study.
Benson M
Neonatal Netw; 2002 Apr; 21(3):7-13. PubMed ID: 12943206
[TBL] [Abstract][Full Text] [Related]
35. Nasal polyposis in pediatric patients with Cornelia de Lange syndrome: endoscopic diagnosis, treatment and follow up in two case reports.
Onesimo R; Santis R; Leoni C; Rigante M; Piastra M; Sforza E; Selicorni A; Zampino G
Ital J Pediatr; 2023 Jul; 49(1):85. PubMed ID: 37455311
[TBL] [Abstract][Full Text] [Related]
36. Cornelia de Lange syndrome in diverse populations.
Dowsett L; Porras AR; Kruszka P; Davis B; Hu T; Honey E; Badoe E; Thong MK; Leon E; Girisha KM; Shukla A; Nayak SS; Shotelersuk V; Megarbane A; Phadke S; Sirisena ND; Dissanayake VHW; Ferreira CR; Kisling MS; Tanpaiboon P; Uwineza A; Mutesa L; Tekendo-Ngongang C; Wonkam A; Fieggen K; Batista LC; Moretti-Ferreira D; Stevenson RE; Prijoles EJ; Everman D; Clarkson K; Worthington J; Kimonis V; Hisama F; Crowe C; Wong P; Johnson K; Clark RD; Bird L; Masser-Frye D; McDonald M; Willems P; Roeder E; Saitta S; Anyane-Yeoba K; Demmer L; Hamajima N; Stark Z; Gillies G; Hudgins L; Dave U; Shalev S; Siu V; Ades A; Dubbs H; Raible S; Kaur M; Salzano E; Jackson L; Deardorff M; Kline A; Summar M; Muenke M; Linguraru MG; Krantz ID
Am J Med Genet A; 2019 Feb; 179(2):150-158. PubMed ID: 30614194
[TBL] [Abstract][Full Text] [Related]
37. Aniridia and Brachmann-de Lange syndrome: a review of ocular surface and anterior segment findings.
Lee WB; Brandt JD; Mannis MJ; Huang CQ; Rabin GJ
Cornea; 2003 Mar; 22(2):178-80. PubMed ID: 12605058
[TBL] [Abstract][Full Text] [Related]
38. Epileptic features in Cornelia de Lange syndrome: case report and literature review.
Pavlidis E; Cantalupo G; Bianchi S; Piccolo B; Pisani F
Brain Dev; 2014 Nov; 36(10):837-43. PubMed ID: 24461912
[TBL] [Abstract][Full Text] [Related]
39. Cornelia de Lange syndrome and congenital diaphragmatic hernia.
Gupta VS; Khan AM; Ebanks AH; Lally PA; Lally KP; Harting MT;
J Pediatr Surg; 2021 Apr; 56(4):697-699. PubMed ID: 32762940
[TBL] [Abstract][Full Text] [Related]
40.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
