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The inv dup (15) or idic (15) syndrome (Tetrasomy 15q).

Battaglia A.

Orphanet J Rare Dis. 2008 Nov 19;3:30. Review.PMID: 19019226 [PubMed - indexed for MEDLINE]Related articlesFree article

The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder.

Battaglia A.

Brain Dev. 2005 Aug;27(5):365-9. Epub 2005 Apr 22. Review.PMID: 16023554 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 9504785 [PubMed - indexed for MEDLINE]Related articles

Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes.

Huang B, Crolla JA, Christian SL, Wolf-Ledbetter ME, Macha ME, Papenhausen PN, Ledbetter DH.

Hum Genet. 1997 Jan;99(1):11-7.PMID: 9003485 [PubMed - indexed for MEDLINE]Related articles

Maternal uniparental disomy in a patient with Prader-Willi syndrome with an additional small inv dup(15) chromosome.

Wang YM, Chuang L, Wang BT, Kuo PL.

J Formos Med Assoc. 2004 Dec;103(12):943-7.PMID: 15624046 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 9109904 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 8069650 [PubMed - indexed for MEDLINE]Related articles

Partial hexasomy of chromosome 15.

Huang B, Bartley J.

Am J Med Genet A. 2003 Sep 1;121A(3):277-80.PMID: 12923871 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 7767656 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 12199736 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 10845741 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 7942854 [PubMed - indexed for MEDLINE]Related articlesFree article

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 11;61(2):182-7.PMID: 8669450 [PubMed - indexed for MEDLINE]Related articles

Triplication of 15q11-q13 with inv dup(15) in a female with developmental delay.

Long FL, Duckett DP, Billam LJ, Williams DK, Crolla JA.

J Med Genet. 1998 May;35(5):425-8.PMID: 9610809 [PubMed - indexed for MEDLINE]Related articlesFree article

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.PMID: 10868780 [PubMed - indexed for MEDLINE]Related articles

Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14.

Ungaro P, Christian SL, Fantes JA, Mutirangura A, Black S, Reynolds J, Malcolm S, Dobyns WB, Ledbetter DH.

J Med Genet. 2001 Jan;38(1):26-34.PMID: 11134237 [PubMed - indexed for MEDLINE]Related articlesFree article

Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.

Leana-Cox J, Jenkins L, Palmer CG, Plattner R, Sheppard L, Flejter WL, Zackowski J, Tsien F, Schwartz S.

Am J Hum Genet. 1994 May;54(5):748-56.PMID: 8178816 [PubMed - indexed for MEDLINE]Related articlesFree article

Interstitial duplications of chromosome region 15q11q13: clinical and molecular characterization.

Repetto GM, White LM, Bader PJ, Johnson D, Knoll JH.

Am J Med Genet. 1998 Sep 1;79(2):82-9.PMID: 9741464 [PubMed - indexed for MEDLINE]Related articles

Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.

Spinner NB, Zackai E, Cheng SD, Knoll JH.

Am J Med Genet. 1995 May 22;57(1):61-5.PMID: 7645601 [PubMed - indexed for MEDLINE]Related articles

Supernumerary tricentric derivative chromosome 15 in two boys with intractable epilepsy: another mechanism for partial hexasomy.

Mann SM, Wang NJ, Liu DH, Wang L, Schultz RA, Dorrani N, Sigman M, Schanen NC.

Hum Genet. 2004 Jul;115(2):104-11. Epub 2004 May 13.PMID: 15141347 [PubMed - indexed for MEDLINE]Related articles