178 related articles for article (PubMed ID: 17337261)
1. Left-ventricular non-compaction in a patient with monosomy 1p36.
Thienpont B; Mertens L; Buyse G; Vermeesch JR; Devriendt K
Eur J Med Genet; 2007; 50(3):233-6. PubMed ID: 17337261
[TBL] [Abstract][Full Text] [Related]
2. Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5-11.1 Mb terminal deletion of 1p36.
Saito S; Kawamura R; Kosho T; Shimizu T; Aoyama K; Koike K; Wada T; Matsumoto N; Kato M; Wakui K; Fukushima Y
Am J Med Genet A; 2008 Nov; 146A(22):2891-7. PubMed ID: 18925681
[TBL] [Abstract][Full Text] [Related]
3. Left-ventricular non-compaction (LVNC): a clinical feature more often observed in terminal deletion 1p36 than previously expected.
Cremer K; Lüdecke HJ; Ruhr F; Wieczorek D
Eur J Med Genet; 2008; 51(6):685-8. PubMed ID: 18721913
[TBL] [Abstract][Full Text] [Related]
4. Monosomy 1p36 deletion syndrome.
Gajecka M; Mackay KL; Shaffer LG
Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):346-56. PubMed ID: 17918734
[TBL] [Abstract][Full Text] [Related]
5. 576 kb deletion in 1p36.33-p36.32 containing SKI is associated with limb malformation, congenital heart disease and epilepsy.
Zhu X; Zhang Y; Wang J; Yang JF; Yang YF; Tan ZP
Gene; 2013 Oct; 528(2):352-5. PubMed ID: 23892090
[TBL] [Abstract][Full Text] [Related]
6. Interstitial 1q43-q43 deletion with left ventricular noncompaction myocardium.
Kanemoto N; Horigome H; Nakayama J; Ichida F; Xing Y; Buonadonna AL; Kanemoto K; Gentile M
Eur J Med Genet; 2006; 49(3):247-53. PubMed ID: 16762826
[TBL] [Abstract][Full Text] [Related]
7. Contiguous ∼16 Mb 1p36 deletion: Dominant features of classical distal 1p36 monosomy with haplo-lethality.
Nicoulaz A; Rubi F; Lieder L; Wolf R; Goeggel-Simonetti B; Steinlin M; Wiest R; Bonel HM; Schaller A; Gallati S; Conrad B
Am J Med Genet A; 2011 Aug; 155A(8):1964-8. PubMed ID: 21739569
[TBL] [Abstract][Full Text] [Related]
8. Epilepsy and neurological findings in 11 individuals with 1p36 deletion syndrome.
Kurosawa K; Kawame H; Okamoto N; Ochiai Y; Akatsuka A; Kobayashi M; Shimohira M; Mizuno S; Wada K; Fukushima Y; Kawawaki H; Yamamoto T; Masuno M; Imaizumi K; Kuroki Y
Brain Dev; 2005 Aug; 27(5):378-82. PubMed ID: 16023556
[TBL] [Abstract][Full Text] [Related]
9. Monosomy 1p36.
Slavotinek A; Shaffer LG; Shapira SK
J Med Genet; 1999 Sep; 36(9):657-63. PubMed ID: 10507720
[TBL] [Abstract][Full Text] [Related]
10. Molecular characterization of a monosomy 1p36 presenting as an Aicardi syndrome phenocopy.
Bursztejn AC; Bronner M; Peudenier S; Grégoire MJ; Jonveaux P; Nemos C
Am J Med Genet A; 2009 Nov; 149A(11):2493-500. PubMed ID: 19842196
[TBL] [Abstract][Full Text] [Related]
11. Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome.
Heilstedt HA; Ballif BC; Howard LA; Lewis RA; Stal S; Kashork CD; Bacino CA; Shapira SK; Shaffer LG
Am J Hum Genet; 2003 May; 72(5):1200-12. PubMed ID: 12687501
[TBL] [Abstract][Full Text] [Related]
12. Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case report.
Nistico' D; Guidolin F; Navarra CO; Bobbo M; Magnolato A; D'Adamo AP; Giorgio E; Pivetta B; Barbi E; Gasparini P; Cadenaro M; Sirchia F
BMC Pediatr; 2020 May; 20(1):201. PubMed ID: 32386509
[TBL] [Abstract][Full Text] [Related]
13. Left Ventricular Non-compaction: Is It Genetic?
Ting TW; Jamuar SS; Brett MS; Tan ES; Cham BW; Lim JY; Law HY; Tan EC; Choo JT; Lai AH
Pediatr Cardiol; 2015 Dec; 36(8):1565-72. PubMed ID: 26108892
[TBL] [Abstract][Full Text] [Related]
14. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
[TBL] [Abstract][Full Text] [Related]
15. Nonrandom association of atrioventricular canal and del (8p) syndrome.
Marino B; Reale A; Giannotti A; Digilio MC; Dallapiccola B
Am J Med Genet; 1992 Feb; 42(4):424-7. PubMed ID: 1609823
[TBL] [Abstract][Full Text] [Related]
16. Del 1p36 syndrome: a newly emerging clinical entity.
Battaglia A
Brain Dev; 2005 Aug; 27(5):358-61. PubMed ID: 16023552
[TBL] [Abstract][Full Text] [Related]
17. Multiple congenital anomalies, thymic dysplasia, severe congenital heart disease, and oligosyndactyly with a deletion of the short arm of chromosome 5.
Taylor MJ; Josifek K
Am J Med Genet; 1981; 9(1):5-11. PubMed ID: 6264787
[TBL] [Abstract][Full Text] [Related]
18. Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: a brief review.
Stockton DW; Ross HL; Bacino CA; Altman CA; Shaffer LG; Lupski JR
Am J Med Genet; 1997 Aug; 71(2):189-93. PubMed ID: 9217220
[TBL] [Abstract][Full Text] [Related]
19. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies.
Gamba BF; Richieri-Costa A; Costa S; Rosenberg C; Ribeiro-Bicudo LA
Mol Genet Genomics; 2015 Dec; 290(6):2213-6. PubMed ID: 26040972
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of monosomy 1p36: a focus on brain abnormalities and a review of the literature.
Campeau PM; Ah Mew N; Cartier L; Mackay KL; Shaffer LG; Der Kaloustian VM; Thomas MA
Am J Med Genet A; 2008 Dec; 146A(23):3062-9. PubMed ID: 19006213
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
