431 related articles for article (PubMed ID: 19852437)
1. Joubert syndrome associated with patent ductus arteriosus in a newborn infant.
Peker E; Kirimi E; Sal E; Ceylan A; Ustyol L; Caksen H
Genet Couns; 2009; 20(3):289-92. PubMed ID: 19852437
[No Abstract] [Full Text] [Related]
2. Joubert syndrome.
Solomon R; Jana AK; Singh S; Biswas A
Indian Pediatr; 2001 Sep; 38(9):1045-9. PubMed ID: 11568384
[No Abstract] [Full Text] [Related]
3. Terminal 2q37 deletion and autistic behaviour.
Lukusa T; Smeets E; Vogels A; Vermeesch JR; Fryns JP
Genet Couns; 2005; 16(2):179-80. PubMed ID: 16080299
[No Abstract] [Full Text] [Related]
4. Cerebral and cerebellar motor activation abnormalities in a subject with Joubert syndrome: functional magnetic resonance imaging (MRI) study.
Parisi MA; Pinter JD; Glass IA; Field K; Maria BL; Chance PF; Mahurin RK; Cramer SC
J Child Neurol; 2004 Mar; 19(3):214-8. PubMed ID: 15119482
[TBL] [Abstract][Full Text] [Related]
5. Familial patent ductus arteriosus: a further case of CHAR syndrome.
Slavotinek A; Clayton-Smith J; Super M
Am J Med Genet; 1997 Aug; 71(2):229-32. PubMed ID: 9217229
[TBL] [Abstract][Full Text] [Related]
6. A VERY RARE CAUSE OF APNEA IN THE NEONATAL PERIOD: JOUBERT SYNDROME.
Demirel G; Yilmaz A; Vatansever B; Karavar H; Gundogdu S; Vatansever S; Turanli G; Tastekin A
Genet Couns; 2016; 27(3):425-428. PubMed ID: 30204974
[No Abstract] [Full Text] [Related]
7. A novel Fryns "Anophthalmia-plus" syndrome associated with primary hypothyroidism.
Akalin I; Senses DA; Ilgin-Ruhi H; Misirlioğlu E; Yalçiner M; Cetinkaya E; Fryns JP; Tükün A
Genet Couns; 2005; 16(2):145-8. PubMed ID: 16080293
[TBL] [Abstract][Full Text] [Related]
8. Acro-cardio-facial syndrome associated with neuroepithelial cyst: a case report.
Sivasli O; Ozer EA; Ozer A; Aydinlioglu H; Helvaci M
Genet Couns; 2007; 18(2):247-50. PubMed ID: 17710878
[TBL] [Abstract][Full Text] [Related]
9. [Cardiac symptoms in 2 patients with Seckel syndrome].
Rappen U; von Brenndorff AI
Monatsschr Kinderheilkd; 1993 Jul; 141(7):584-6. PubMed ID: 8413337
[TBL] [Abstract][Full Text] [Related]
10. Norwood procedure combined with the Starnes procedure.
Nakata T; Fujimoto Y; Hirose K; Tosaka Y; Ide Y; Sakamoto K
Ann Thorac Surg; 2008 Oct; 86(4):1378-80. PubMed ID: 18805206
[TBL] [Abstract][Full Text] [Related]
11. Schinzel-Giedion syndrome. A patient with hypothyroidism and diabetes insipidus.
Santos H; Cordeiro I; Medeira A; Mendonça E; Antunes NL; Rosa FC
Genet Couns; 1994; 5(2):187-9. PubMed ID: 7917131
[TBL] [Abstract][Full Text] [Related]
12. A case of cranial meningocele associated with Joubert syndrome.
Suzuki T; Hakozaki M; Kubo N; Kuroda K; Ogawa A
Childs Nerv Syst; 1996 May; 12(5):280-2. PubMed ID: 8737806
[TBL] [Abstract][Full Text] [Related]
13. Symptomatic neonates with Ebstein anomaly.
Pflaumer A; Eicken A; Augustin N; Hess J
J Thorac Cardiovasc Surg; 2004 Apr; 127(4):1208-9. PubMed ID: 15052228
[No Abstract] [Full Text] [Related]
14. [A newborn infant with the xxxxy-syndrome].
Muis N; Cats BP; Ippel PF; Beemer FA
Tijdschr Kindergeneeskd; 1982 Aug; 50(4):112-6. PubMed ID: 7135379
[TBL] [Abstract][Full Text] [Related]
15. The acrofacial dysostoses--a wide spectrum of overlapping phenotypes.
Dimitrov B; Balikova I; Bradinova I; Zahariev D; Popova A; Simeonov E; De Smet L; Devriendt K; Fryns JP
Genet Couns; 2005; 16(2):181-6. PubMed ID: 16080300
[No Abstract] [Full Text] [Related]
16. Toriello-Carey syndrome in a Turkish newborn.
Uras N; Sandal G; Oguz S; Aydemir O; Erdeve O; Dilmen U
Genet Couns; 2009; 20(3):243-7. PubMed ID: 19852430
[TBL] [Abstract][Full Text] [Related]
17. Char syndrome (unusual mouth, patent ductus arteriosus, phalangeal anomalies).
Temple IK
Clin Dysmorphol; 1992 Jan; 1(1):17-21. PubMed ID: 1342853
[TBL] [Abstract][Full Text] [Related]
18. Partial deletion of chromosome 12q is not usually associated with CFC syndrome.
Zollino M; Neri G
Am J Med Genet; 2000 Nov; 95(3):296. PubMed ID: 11102944
[No Abstract] [Full Text] [Related]
19. Revisit on a distinctive chromosome 1p36 deletion syndrome: report of one case and review of the English literature.
Lee ML; Tsao LY; Wang BT; Lee MH; Chiu IS
Int J Cardiol; 2004 Sep; 96(3):477-80. PubMed ID: 15301904
[No Abstract] [Full Text] [Related]
20. Hyperekplexia in a neonate: a novel finding in Fukuyama type congenital muscular dystrophy.
Tunc T; Mungan IA; Okulu E; Tiras ST; Tekin M; Atasay B; Arsan S; Turmen T
Genet Couns; 2009; 20(3):275-9. PubMed ID: 19852435
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
