244 related articles for article (PubMed ID: 10868780)
1. The syndrome of inv dup (15): clinical, electroencephalographic, and imaging findings.
Buoni S; Sorrentino L; Farnetani MA; Pucci L; Fois A
J Child Neurol; 2000 Jun; 15(6):380-5. PubMed ID: 10868780
[TBL] [Abstract][Full Text] [Related]
2. Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan.
Hou JW; Wang TR
Eur J Pediatr; 1998 Feb; 157(2):122-7. PubMed ID: 9504785
[TBL] [Abstract][Full Text] [Related]
3. The inv dup (15) or idic (15) syndrome (Tetrasomy 15q).
Battaglia A
Orphanet J Rare Dis; 2008 Nov; 3():30. PubMed ID: 19019226
[TBL] [Abstract][Full Text] [Related]
4. Symptomatic generalized epilepsy associated with an inverted duplication of chromosome 15.
Takeda Y; Baba A; Nakamura F; Ito M; Honma H; Koyama T
Seizure; 2000 Mar; 9(2):145-50. PubMed ID: 10845741
[TBL] [Abstract][Full Text] [Related]
5. The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsy.
Battaglia A; Gurrieri F; Bertini E; Bellacosa A; Pomponi MG; Paravatou-Petsotas M; Mazza S; Neri G
Neurology; 1997 Apr; 48(4):1081-6. PubMed ID: 9109904
[TBL] [Abstract][Full Text] [Related]
6. Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.
Flejter WL; Bennett-Baker PE; Ghaziuddin M; McDonald M; Sheldon S; Gorski JL
Am J Med Genet; 1996 Jan; 61(2):182-7. PubMed ID: 8669450
[TBL] [Abstract][Full Text] [Related]
7. Relationship between clinical and genetic features in "inverted duplicated chromosome 15" patients.
Borgatti R; Piccinelli P; Passoni D; Dalprà L; Miozzo M; Micheli R; Gagliardi C; Balottin U
Pediatr Neurol; 2001 Feb; 24(2):111-6. PubMed ID: 11275459
[TBL] [Abstract][Full Text] [Related]
8. Mild generalized epilepsy and developmental disorder associated with large inv dup(15).
Chifari R; Guerrini R; Pierluigi M; Cavani S; Sgrò V; Elia M; Canger R; Canevini MP
Epilepsia; 2002 Sep; 43(9):1096-100. PubMed ID: 12199736
[TBL] [Abstract][Full Text] [Related]
9. The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder.
Battaglia A
Brain Dev; 2005 Aug; 27(5):365-9. PubMed ID: 16023554
[TBL] [Abstract][Full Text] [Related]
10. Clinical and molecular analysis of five inv dup(15) patients.
Robinson WP; Binkert F; Giné R; Vazquez C; Müller W; Rosenkranz W; Schinzel A
Eur J Hum Genet; 1993; 1(1):37-50. PubMed ID: 8069650
[TBL] [Abstract][Full Text] [Related]
11. Inv dup (15) with mental retardation but few dysmorphic features.
Gilmore DH; Boyd E; McClure JP; Batstone P; Connor JM
J Med Genet; 1984 Jun; 21(3):221-3. PubMed ID: 6748020
[TBL] [Abstract][Full Text] [Related]
12. Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome.
Chen CP; Lin SP; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Oct; 55(5):728-732. PubMed ID: 27751425
[TBL] [Abstract][Full Text] [Related]
13. Inverted duplication of chromosome 15: inv dup (15).
Enzenauer RW; Reinker KA
Mil Med; 1986 Aug; 151(8):440-1. PubMed ID: 3093928
[No Abstract] [Full Text] [Related]
14. Infantile spasms associated with proximal duplication of chromosome 15q.
Bingham PM; Spinner NB; Sovinsky L; Zackai EH; Chance PF
Pediatr Neurol; 1996 Sep; 15(2):163-5. PubMed ID: 8888053
[TBL] [Abstract][Full Text] [Related]
15. Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients.
Cheng SD; Spinner NB; Zackai EH; Knoll JH
Am J Hum Genet; 1994 Oct; 55(4):753-9. PubMed ID: 7942854
[TBL] [Abstract][Full Text] [Related]
16. Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.
Miller DT; Shen Y; Weiss LA; Korn J; Anselm I; Bridgemohan C; Cox GF; Dickinson H; Gentile J; Harris DJ; Hegde V; Hundley R; Khwaja O; Kothare S; Luedke C; Nasir R; Poduri A; Prasad K; Raffalli P; Reinhard A; Smith SE; Sobeih MM; Soul JS; Stoler J; Takeoka M; Tan WH; Thakuria J; Wolff R; Yusupov R; Gusella JF; Daly MJ; Wu BL
J Med Genet; 2009 Apr; 46(4):242-8. PubMed ID: 18805830
[TBL] [Abstract][Full Text] [Related]
17. Inv dup(15) supernumerary marker chromosomes.
Webb T
J Med Genet; 1994 Aug; 31(8):585-94. PubMed ID: 7815414
[No Abstract] [Full Text] [Related]
18. Simultaneous formation of inv dup(15) and dup(15q) in a girl with developmental delay: origin of the abnormal chromosomes.
Abeliovich D; Dagan J; Werner M; Lerer I; Shapira Y; Meiner V
Eur J Hum Genet; 1995; 3(1):49-55. PubMed ID: 7767656
[TBL] [Abstract][Full Text] [Related]
19. Cytogenetic characterization of an extra structurally abnormal chromosome associated with severe mental retardation: inv dup (15) (q13).
Gorla N; Slavutsky I; Lisanti J; Pedrazzini E; Vanella L; Larripa I
Hereditas; 1998; 129(1):1-5. PubMed ID: 9868924
[TBL] [Abstract][Full Text] [Related]
20. Inv dup (15): is the electroclinical phenotype helpful for this challenging clinical diagnosis?
Valente KD; Freitas A; Fridman C; Varela M; Silva AE; Fett AC; Koiffmann CP
Clin Neurophysiol; 2006 Apr; 117(4):803-9. PubMed ID: 16495142
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
