148 related articles for article (PubMed ID: 35021179)
21. The 18q deletion syndrome and analysis of the critical region for orofacial cleft at 18q22.3.
Dostal A; Nemeckova J; Gaillyova R
J Craniomaxillofac Surg; 2009 Jul; 37(5):272-5. PubMed ID: 19157891
[TBL] [Abstract][Full Text] [Related]
22. Intellectual disability associated with craniofacial dysmorphism, cleft palate, and congenital heart defect due to a de novo MEIS2 mutation: A clinical longitudinal study.
Gangfuß A; Yigit G; Altmüller J; Nürnberg P; Czeschik JC; Wollnik B; Bögershausen N; Burfeind P; Wieczorek D; Kaiser F; Roos A; Kölbel H; Schara-Schmidt U; Kuechler A
Am J Med Genet A; 2021 Apr; 185(4):1216-1221. PubMed ID: 33427397
[TBL] [Abstract][Full Text] [Related]
23. De novo 5q14.3 translocation 121.5-kb upstream of MEF2C in a patient with severe intellectual disability and early-onset epileptic encephalopathy.
Saitsu H; Igarashi N; Kato M; Okada I; Kosho T; Shimokawa O; Sasaki Y; Nishiyama K; Tsurusaki Y; Doi H; Miyake N; Harada N; Hayasaka K; Matasumoto N
Am J Med Genet A; 2011 Nov; 155A(11):2879-84. PubMed ID: 21990267
[TBL] [Abstract][Full Text] [Related]
24. Interstitial deletion 5q14.3q21.3 with MEF2C haploinsufficiency and mild phenotype: when more is less.
Tonk V; Kyhm JH; Gibson CE; Wilson GN
Am J Med Genet A; 2011 Jun; 155A(6):1437-41. PubMed ID: 21567930
[TBL] [Abstract][Full Text] [Related]
25. Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation.
Osoegawa K; Vessere GM; Utami KH; Mansilla MA; Johnson MK; Riley BM; L'Heureux J; Pfundt R; Staaf J; van der Vliet WA; Lidral AC; Schoenmakers EF; Borg A; Schutte BC; Lammer EJ; Murray JC; de Jong PJ
J Med Genet; 2008 Feb; 45(2):81-6. PubMed ID: 17873121
[TBL] [Abstract][Full Text] [Related]
26. Multiple malformation syndrome including cleft lip and palate and cardiac abnormalities due to an interstitial deletion of chromosome 12q.
Meinecke P; Meinecke R
J Med Genet; 1987 Mar; 24(3):187. PubMed ID: 3573007
[No Abstract] [Full Text] [Related]
27. 22q11 Deletion in children with cleft lip and palate--is routine screening justified?
Bashir MA; Hodgkinson PD; Montgomery T; Splitt M
J Plast Reconstr Aesthet Surg; 2008; 61(2):130-2. PubMed ID: 17707704
[TBL] [Abstract][Full Text] [Related]
28. 5q14.3 neurocutaneous syndrome: a novel continguous gene syndrome caused by simultaneous deletion of RASA1 and MEF2C.
Carr CW; Zimmerman HH; Martin CL; Vikkula M; Byrd AC; Abdul-Rahman OA
Am J Med Genet A; 2011 Jul; 155A(7):1640-5. PubMed ID: 21626678
[TBL] [Abstract][Full Text] [Related]
29. De novo interstitial deletion of 1q32.2-q32.3 including the entire IRF6 gene in a patient with oral cleft and other dysmorphic features.
Salahshourifar I; Halim AS; Sulaiman WA; Ariffin R; Naili Muhamad Nor N; Zilfalil BA
Cytogenet Genome Res; 2011; 134(2):83-7. PubMed ID: 21447942
[TBL] [Abstract][Full Text] [Related]
30. 22q11.2 Deletion Syndrome in Colombian Patients With Syndromic Cleft Lip and/or Palate.
Carpeta S; Pineda T; Martínez MC; Osorio G; Porras-Hurtado GL; Rojas J; Zarante I; Moreno-Niño OM
Cleft Palate Craniofac J; 2019 Jan; 56(1):116-122. PubMed ID: 29652534
[TBL] [Abstract][Full Text] [Related]
31. [Van der Woude syndrome in combination with ring chromosome 18].
Kalker U; Gabriel M; Jacobi G
Monatsschr Kinderheilkd; 1988 Feb; 136(2):95-8. PubMed ID: 3367915
[TBL] [Abstract][Full Text] [Related]
32. Chromosome 22q11 deletion and other chromosome aberrations in cases with cleft palate, congenital heart defects and/or mental disability. A survey based on the Danish Facial Cleft Register.
Brøndum-Nielsen K; Christensen K
Clin Genet; 1996 Sep; 50(3):116-20. PubMed ID: 8946108
[TBL] [Abstract][Full Text] [Related]
33. Cardiofacioneurodevelopmental syndrome: Report of a novel patient and expansion of the phenotype.
Abdalla E; Alawi M; Meinecke P; Kutsche K; Harms FL
Am J Med Genet A; 2022 Aug; 188(8):2448-2453. PubMed ID: 35451546
[TBL] [Abstract][Full Text] [Related]
34. Report of a patient with developmental delay, hearing loss, growth retardation, and cleft lip and palate and a deletion of 7q34-36.1: review of distal 7q deletions.
Rush ET; Stevens JM; Sanger WG; Olney AH
Am J Med Genet A; 2013 Jul; 161A(7):1726-32. PubMed ID: 23696251
[TBL] [Abstract][Full Text] [Related]
35. Van der Woude syndrome: a review of 11 cases seen at the Lagos University Teaching Hospital.
James O; Adeyemo WL; Emeka CI; Ogunlewe MO; Ladeinde AL; Butali A
Afr J Paediatr Surg; 2014; 11(1):52-5. PubMed ID: 24647295
[TBL] [Abstract][Full Text] [Related]
36. An autosomal dominant syndrome of uveal colobomata, cleft lip and palate, and mental retardation.
Kingston HM; Harper PS; Jones PW
J Med Genet; 1982 Dec; 19(6):444-6. PubMed ID: 7154042
[TBL] [Abstract][Full Text] [Related]
37. Severe epilepsy, retardation, and dysmorphic features with a 2q deletion including SCN1A and SCN2A.
Pereira S; Vieira JP; Barroca F; Roll P; Carvalhas R; Cau P; Sequeira S; Genton P; Szepetowski P
Neurology; 2004 Jul; 63(1):191-2. PubMed ID: 15249644
[No Abstract] [Full Text] [Related]
38. Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones.
Chen CP; Chen CY; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2017 Dec; 56(6):821-826. PubMed ID: 29241927
[TBL] [Abstract][Full Text] [Related]
39. Syndactyly, ectodermal dysplasia, and cleft lip/palate.
Zlotogora J
J Med Genet; 1994 Dec; 31(12):957-9. PubMed ID: 7891379
[No Abstract] [Full Text] [Related]
40. MEIS2 involvement in cardiac development, cleft palate, and intellectual disability.
Louw JJ; Corveleyn A; Jia Y; Hens G; Gewillig M; Devriendt K
Am J Med Genet A; 2015 May; 167A(5):1142-6. PubMed ID: 25712757
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]