176 related articles for article (PubMed ID: 10779849)
21. Bladder carcinoma in Costello syndrome: report on a patient born to consanguineous parents and review.
Franceschini P; Licata D; Di Cara G; Guala A; Bianchi M; Ingrosso G; Franceschini D
Am J Med Genet; 1999 Sep; 86(2):174-9. PubMed ID: 10449656
[TBL] [Abstract][Full Text] [Related]
22. Anorectal anomalies, diaphragmatic defect, cleft palate, lower lip pits, hypopigmentation and hypogammaglobulinemia A in Kabuki syndrome: a rare combination.
Abdel-Salam GM; Afifi HH; Eid MM; el-Badry TH; Kholoussi NM
Genet Couns; 2008; 19(3):309-17. PubMed ID: 18990987
[TBL] [Abstract][Full Text] [Related]
23. [Studies on the pathology of oculo-cerebro-renal syndrome (Lowe)].
Arrigoni A; Zunin C
Pathologica; 1974; 66(953-954):113-24. PubMed ID: 4418886
[No Abstract] [Full Text] [Related]
24. Cutis laxa in Kabuki make-up syndrome.
Vaccaro M; Salpietro DC; Briuglia S; Merlino MV; Guarneri F; Dallapiccola B
J Am Acad Dermatol; 2005 Nov; 53(5 Suppl 1):S247-51. PubMed ID: 16227101
[TBL] [Abstract][Full Text] [Related]
25. Anesthesia management in Kabuki make-up syndrome.
Sivaci R; Kahveci OK; Celik M; Altuntas A; Solak M
Saudi Med J; 2005 Dec; 26(12):1980-2. PubMed ID: 16380786
[TBL] [Abstract][Full Text] [Related]
26. [Kabuki syndrome, a congenital syndrome with multiple anomalies].
den Biggelaar AM; Kuijpers-Jagtman AM; Bergé SJ; Katsaros C
Ned Tijdschr Tandheelkd; 2006 Dec; 113(12):516-9. PubMed ID: 17193989
[TBL] [Abstract][Full Text] [Related]
27. [Hypomelanosis of Ito. A possibly under-diagnosed heterogeneous neurocutaneous syndrome].
Gómez-Lado C; Eirís-Puñal J; Blanco-Barca O; del Río-Latorre E; Fernández-Redondo V; Castro-Gago M
Rev Neurol; 2004 Feb 1-15; 38(3):223-8. PubMed ID: 14963848
[TBL] [Abstract][Full Text] [Related]
28. [Kabuki make-up (Niikawa-Kuroki) syndrome].
Niikawa N
Ryoikibetsu Shokogun Shirizu; 2001; (36):484-5. PubMed ID: 11596445
[No Abstract] [Full Text] [Related]
29. Kabuki makeup syndrome (Niikawa-Kuroki syndrome) in a black child.
PeBenito R; Ferretti C
Ann Ophthalmol; 1989 Aug; 21(8):312-5. PubMed ID: 2802456
[TBL] [Abstract][Full Text] [Related]
30. Hand anomalies in Russell Silver syndrome.
Lahiri A; Lester R
J Plast Reconstr Aesthet Surg; 2009 Apr; 62(4):462-5. PubMed ID: 18171637
[TBL] [Abstract][Full Text] [Related]
31. Uncombable hair syndrome, mental retardation, single palmar crease and arched palate in a patient with neurofibromatosis type I.
Schena D; Germi L; Zamperetti MR; Darra F; Giacopuzzi S; Girolomoni G
Pediatr Dermatol; 2007; 24(5):E73-5. PubMed ID: 17958786
[TBL] [Abstract][Full Text] [Related]
32. Ophthalmologic findings in the Cornelia de Lange syndrome.
Levin AV; Seidman DJ; Nelson LB; Jackson LG
J Pediatr Ophthalmol Strabismus; 1990; 27(2):94-102. PubMed ID: 2348318
[TBL] [Abstract][Full Text] [Related]
33. T-cell clonality and myelodysplasia without chromosomal fragility in a patient with features of Seckel syndrome.
Chanan-Khan A; Holkova B; Perle MA; Reich E; Wu CD; Inghirami G; Takeshita K
Haematologica; 2003 May; 88(5):ECR14. PubMed ID: 12745283
[TBL] [Abstract][Full Text] [Related]
34. [The De Barsy syndrome].
Hoekx J; Smeitink J; Brunner H; Monnens L
Tijdschr Kindergeneeskd; 1989 Apr; 57(2):53-7. PubMed ID: 2741159
[TBL] [Abstract][Full Text] [Related]
35. Ocular manifestations in mentally retarded children.
Kalra A; Bhatia R; Kalra K; Dayal RS; Dutt T; Pandey DJ; Singh YP; Misra MN
Indian Pediatr; 1987 May; 24(5):409-13. PubMed ID: 3679492
[No Abstract] [Full Text] [Related]
36. [Hypertrophic cardiomyopathy (probably secondary) in an infant with Stickler's syndrome. The physiopathological aspects].
Distefano G; Falsaperla R; Sciacca P; Sorge G; Parisi MG; Greco F; Pavone L
Pediatr Med Chir; 1993; 15(2):209-12. PubMed ID: 8321727
[TBL] [Abstract][Full Text] [Related]
37. Expanding the clinical picture of Simpson-Golabi-Behmel syndrome.
Young EL; Wishnow R; Nigro MA
Pediatr Neurol; 2006 Feb; 34(2):139-42. PubMed ID: 16458828
[TBL] [Abstract][Full Text] [Related]
38. [Smith-Lemli-Opitz Syndrome; endocrinologic study (author's transl)].
Muñoz Calvo MT; Ceñal González MJ; Parra Martínez I; Hervás Olivares F; Nieto Cuartero JA; Lestache RG
An Esp Pediatr; 1981 Nov; 15(5):498-502. PubMed ID: 7332154
[TBL] [Abstract][Full Text] [Related]
39. [Ocular findings in a peculiar type of mucolipidosis called nephrosialidosis].
Dufier JL; Dhermy P; Limon S; Maroteaux P; Mande R; Polliot L
J Fr Ophtalmol; 1980; 3(4):247-56. PubMed ID: 7440902
[TBL] [Abstract][Full Text] [Related]
40. The spectrum of congenital cardiac malformations encountered in six children with Kabuki syndrome.
McMahon CJ; Reardon W
Cardiol Young; 2006 Feb; 16(1):30-3. PubMed ID: 16454874
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
