324 related articles for article (PubMed ID: 19227428)
1. A well-documented trisomy 13 case presenting with a number of common and uncommon features of the syndrome.
Balci S; Güçer S; Orhan D; Karagöz T
Turk J Pediatr; 2008; 50(6):595-9. PubMed ID: 19227428
[TBL] [Abstract][Full Text] [Related]
2. Trisomy 18 with multiple rare malformations: report of one case.
Su PH; Chen JY; Hsu CH; Chen SJ; Chan SW; Lin LL
Acta Paediatr Taiwan; 2007; 48(5):272-5. PubMed ID: 18254577
[TBL] [Abstract][Full Text] [Related]
3. [A rare combination of partial trisomy 9 with pulmonary atresia].
Nekarda T; Kececioglu D; Kehl HG; Gehrmann J; Miny P; Vogt J
Klin Padiatr; 1997; 209(3):127-9. PubMed ID: 9244820
[TBL] [Abstract][Full Text] [Related]
4. Berry syndrome with trisomy 13.
Sharma J; Saleh M; Das BB
Pediatr Cardiol; 2002; 23(2):205-9. PubMed ID: 11889536
[TBL] [Abstract][Full Text] [Related]
5. [Intestinal malformations and congenital heart diseases].
Voisin M; Galifer RB; Kadiri T; Grolleau R; Dumas R; Jean R
Arch Mal Coeur Vaiss; 1987 Apr; 80(4):524-8. PubMed ID: 3113372
[TBL] [Abstract][Full Text] [Related]
6. Constellation of congenital abnormalities in an infant: a new syndrome or tissue-specific mosaicism for trisomy 18?
Shashi V; Golden WL; von Kap-Herr C; Wilson WG
Am J Med Genet; 1996 Mar; 62(1):38-41. PubMed ID: 8779322
[TBL] [Abstract][Full Text] [Related]
7. Multiple congenital malformations in two sibs reminiscent of hydrolethalus and pseudotrisomy 13 syndromes.
Dincsoy MY; Salih MA; al-Jurayyan N; al Saadi M; Patel PJ
Am J Med Genet; 1995 Apr; 56(3):317-21. PubMed ID: 7778599
[TBL] [Abstract][Full Text] [Related]
8. [Pathological anatomy of Edwards' syndrome (trisomy 18)].
Laziuk GI; Lur'e IV; Kravtsova GI; Kirillova IA; Nedz'ved' MK; Puchkov GF
Arkh Patol; 1976; 38(6):16-22. PubMed ID: 1021059
[TBL] [Abstract][Full Text] [Related]
9. Splenopancreatic field abnormality is not unique to trisomy 13.
Peres LC; Barbosa GH; Careta RS; Nassif CM; de Pina-Neto JM; Giuliani LR; Martinhago CD; Gomy I
Pediatr Dev Pathol; 2004; 7(1):91-4. PubMed ID: 15255041
[TBL] [Abstract][Full Text] [Related]
10. [Fryns syndrome--pre and postnatal diagnosis].
Dix U; Beudt U; Langenbeck U
Z Geburtshilfe Perinatol; 1991; 195(6):280-4. PubMed ID: 1776320
[TBL] [Abstract][Full Text] [Related]
11. Atypical manifestations of two cases of trisomy 9 syndrome: rethinking development delay.
Saneto RP; Applegate KE; Frankel DG
Am J Med Genet; 1998 Oct; 80(1):42-5. PubMed ID: 9800910
[TBL] [Abstract][Full Text] [Related]
12. Spectrum of clinical and autopsy findings in trisomy 18 syndrome.
Moerman P; Fryns JP; Goddeeris P; Lauweryns JM
J Genet Hum; 1982 Mar; 30(1):17-38. PubMed ID: 7130954
[TBL] [Abstract][Full Text] [Related]
13. Trisomy 17 in a baboon (Papio hamadryas) with polydactyly, patent foramen ovale and pyelectasis.
Moore CM; Hubbard GB; Dick E; Dunn BG; Raveendran M; Rogers J; Williams V; Gomez JJ; Butler SD; Leland MM; Schlabritz-Loutsevitch NE
Am J Primatol; 2007 Oct; 69(10):1105-18. PubMed ID: 17330307
[TBL] [Abstract][Full Text] [Related]
14. Biliary atresia splenic malformation syndrome--is it a result of embryonically midline rotational defects? A case report.
Deveci MS; Deveci G
J Pediatr Surg; 2000 Sep; 35(9):1377-80. PubMed ID: 10999706
[TBL] [Abstract][Full Text] [Related]
15. Maternal origin and clinical findings in a case with trisomy 22.
Mihçi E; Taçoy S; Yakut S; Ongun H; Keser I; Kiliçarslan B; Bağci G; Lüleci G
Turk J Pediatr; 2007; 49(3):322-6. PubMed ID: 17990591
[TBL] [Abstract][Full Text] [Related]
16. Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis.
Hartmann A; Hofmann UB; Hoehn H; Broecker EB; Hamm H
Pediatr Dermatol; 2004; 21(6):636-41. PubMed ID: 15575846
[TBL] [Abstract][Full Text] [Related]
17. [Ventricular septal defect, pulmonary hypertension and 3C (cranio-cerebello-cardiac) syndrome: report of a case].
Nakayama M; Kado M; Ishikawa H; Kondou H
Kyobu Geka; 2010 May; 63(5):407-9. PubMed ID: 20446611
[TBL] [Abstract][Full Text] [Related]
18. Association of severe autosomal recessive osteopetrosis and Dandy-Walker syndrome with agenesis of the corpus callosum.
Ben Hamouda H; Sfar MN; Braham R; Ben Salah M; Ayadi A; Soua H; Hamza H; Sfar MT
Acta Orthop Belg; 2001 Dec; 67(5):528-32. PubMed ID: 11822087
[TBL] [Abstract][Full Text] [Related]
19. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
Aglan MS; Kamel AK; Helmy NA
Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
[TBL] [Abstract][Full Text] [Related]
20. Edwards syndrome with double trisomy.
Tennakoon J; Kandasamy Y; Alcock G; Koh TH
Singapore Med J; 2008 Jul; 49(7):e190-1. PubMed ID: 18695855
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]