These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
95 related articles for article (PubMed ID: 8350593)
1. [Holt-Oram syndrome in combination with reciprocal translocation, lung hypoplasia and cardiomyopathy]. Kullmann F; Koch R; Feichtinger W; Giesen H; Schmid M; Grimm T Klin Padiatr; 1993; 205(3):185-9. PubMed ID: 8350593 [TBL] [Abstract][Full Text] [Related]
2. [Comment on F. Kullmann, R. Koch, W. Feichtinger, H. Giesen, M. Schmid, T. Grimm, Holt-Oram syndrome with reciprocal translocation, pulmonary hypoplasia and cardiomyopathy]. Hoeffel JC Klin Padiatr; 1995; 207(3):130. PubMed ID: 7623431 [No Abstract] [Full Text] [Related]
3. [Diagnosis of familial Holt-Oram syndrome]. Lehner R; Wenzl R; Vanura H; Frank W; Safar P; Husslein P Z Geburtshilfe Perinatol; 1994 Aug; 198(4):143-9. PubMed ID: 7975801 [TBL] [Abstract][Full Text] [Related]
4. Perinatal/neonatal case presentation: unexpected severe respiratory insufficiency in a newborn with Holt-Oram Syndrome. Smets K; Mortier G; Zecic A J Perinatol; 2005 Nov; 25(11):745-6. PubMed ID: 16252013 [TBL] [Abstract][Full Text] [Related]
5. Variable clinical expression of Holt-Oram syndrome in three generations. Oğur G; Gül D; Lenk MK; Imirzalioğlu N; Alpay F; Oğur E Turk J Pediatr; 1998; 40(4):613-8. PubMed ID: 10028874 [TBL] [Abstract][Full Text] [Related]
6. [Holt-Oram syndrome. Presentation of two cases (author's transl)]. Ferriols Gil EJ; Fayos Soler JL; Elorza Arizmendi J; Alvarez Angel V An Esp Pediatr; 1981 Oct; 15(4):378-82. PubMed ID: 7337303 [TBL] [Abstract][Full Text] [Related]
7. Asplenia syndrome in a child with a balanced reciprocal translocation of chromosomes 11 and 20 [46,XX,t(11;20)(q13.1;q13.13)]. Freeman SB; Muralidharan K; Pettay D; Blackston RD; May KM Am J Med Genet; 1996 Feb; 61(4):340-4. PubMed ID: 8834045 [TBL] [Abstract][Full Text] [Related]
8. A neonate with ectodermal dysplasia ectrodactyly clefting syndrome and ventricular septal defect. Ram SP; Noor AR; Ariffin WA; Ariffin NA Singapore Med J; 1994 Apr; 35(2):205-7. PubMed ID: 7939823 [TBL] [Abstract][Full Text] [Related]
10. Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13). Krüger G; Götz J; Kvist U; Dunker H; Erfurth F; Pelz L; Zech L Am J Med Genet; 1989 Mar; 32(3):411-6. PubMed ID: 2729360 [TBL] [Abstract][Full Text] [Related]
11. [TAR syndrome (congenital thrombocytopenia and aplasia of the radial bones) in a 5-months-old boy]. Midro AT; Iwaszkiewicz-Pawłowska A; Puchnarewicz A; Debek K Wiad Lek; 1992 Jan; 45(1-2):66-9. PubMed ID: 1295244 [TBL] [Abstract][Full Text] [Related]
12. Proximal trisomy of 1q mosaicism in a girl with hypertrophic cardiomyopathy associated with Wolff-Parkinson-White syndrome and multiple congenital anomalies. Hirshfeld AB; Thompson WR; Patel A; Boone LB; Murphy AM Am J Med Genet; 2001 May; 100(4):264-8. PubMed ID: 11343316 [TBL] [Abstract][Full Text] [Related]
13. Recurrent tetraamelia and pulmonary hypoplasia with multiple malformations in sibs. Rosenak D; Ariel I; Arnon J; Diamant YZ; Ben Chetrit A; Nadjari M; Zilberman R; Yaffe H; Cohen T; Ornoy A Am J Med Genet; 1991 Jan; 38(1):25-8. PubMed ID: 2012129 [TBL] [Abstract][Full Text] [Related]
14. Holt-Oram syndrome presenting as agenesis of the left pericardium. Dias RR; Albuquerque JM; Pereira AC; Stolf NA; Krieger JE; Mady C; Oliveira SA Int J Cardiol; 2007 Jan; 114(1):98-100. PubMed ID: 16376438 [TBL] [Abstract][Full Text] [Related]
15. Holt-Oram syndrome in four half-siblings with unaffected parents: brief clinical report. Braulke I; Herzog S; Thies U; Zoll B Clin Genet; 1991 Apr; 39(4):241-4. PubMed ID: 2070544 [TBL] [Abstract][Full Text] [Related]
16. [Holt-Oram syndrome with chromosomopathy (author's transl)]. González Espinosa C; Artiles Pérez L; García Báez M; Otero Gómez A; García Miranda JL An Esp Pediatr; 1982 Jan; 16(1):77-81. PubMed ID: 7081854 [TBL] [Abstract][Full Text] [Related]
17. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation. Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413 [TBL] [Abstract][Full Text] [Related]
18. Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family. Li QY; Newbury-Ecob RA; Terrett JA; Wilson DI; Curtis AR; Yi CH; Gebuhr T; Bullen PJ; Robson SC; Strachan T; Bonnet D; Lyonnet S; Young ID; Raeburn JA; Buckler AJ; Law DJ; Brook JD Nat Genet; 1997 Jan; 15(1):21-9. PubMed ID: 8988164 [TBL] [Abstract][Full Text] [Related]
19. Association of atrial-ventricular septal defect, blepharophimosis, anal and radial defects in sibs: a new syndrome? Houlston RS; Ironton R; Temple IK Genet Couns; 1994; 5(1):93-6. PubMed ID: 8031543 [No Abstract] [Full Text] [Related]
20. Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome. Basson CT; Bachinsky DR; Lin RC; Levi T; Elkins JA; Soults J; Grayzel D; Kroumpouzou E; Traill TA; Leblanc-Straceski J; Renault B; Kucherlapati R; Seidman JG; Seidman CE Nat Genet; 1997 Jan; 15(1):30-5. PubMed ID: 8988165 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]