Literature DB >> 7815414

Inv dup(15) supernumerary marker chromosomes.

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Year:  1994        PMID： 7815414      PMCID： PMC1050018          DOI： 10.1136/jmg.31.8.585

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  50 in total

1.  Two extra inv dup(15) chromosomes and male infertility: second case.

Authors:  E Manenti
Journal:  Am J Med Genet       Date:  1992-02-01

2.  Characterization of seven DA/DAPI-positive bisatellited marker chromosomes by in situ hybridization.

Authors:  R Plattner; N A Heerema; S R Patil; P N Howard-Peebles; C G Palmer
Journal:  Hum Genet       Date:  1991-07       Impact factor: 4.132

3.  The origin and behavior of two isodicentric bisatellited chromosomes.

Authors:  D L Van Dyke; L Weiss; M Logan; G S Pai
Journal:  Am J Hum Genet       Date:  1977-05       Impact factor: 11.025

4.  Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15.

Authors:  R R Schreck; W R Breg; B F Erlanger; O J Miller
Journal:  Hum Genet       Date:  1977-04-07       Impact factor: 4.132

5.  Bisatellited extra small metacentric chromosome in newborns.

Authors:  U Friedrich; J Nielsen
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

6.  A case of Prader-Willi syndrome in a girl with a small extra chromosome.

Authors:  M A Ridler; O Garrod; J M Berg
Journal:  Acta Paediatr Scand       Date:  1971-03

7.  Identification of a marker chromosome as inv dup(15) by molecular analysis.

Authors:  Y Shibuya; H Tonoki; N Kajii; N Niikawa
Journal:  Clin Genet       Date:  1991-09       Impact factor: 4.438

8.  Cytogenetic and clinical studies in five cases of inv dup(15).

Authors:  L Wisniewski; T Hassold; J Heffelfinger; J V Higgins
Journal:  Hum Genet       Date:  1979-09       Impact factor: 4.132

9.  Prader-Willi syndrome and chromosomal mosaicism 46,XY/47,XY,+mar in two cases.

Authors:  K F Michaelsen; C Lundsteen; F J Hansen
Journal:  Clin Genet       Date:  1979-09       Impact factor: 4.438

10.  Clinical and molecular analysis of five inv dup(15) patients.

Authors:  W P Robinson; F Binkert; R Giné; C Vazquez; W Müller; W Rosenkranz; A Schinzel
Journal:  Eur J Hum Genet       Date:  1993       Impact factor: 4.246
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  21 in total

1.  Inherited DNA amplification of the proximal 15q region: cytogenetic and molecular studies.

Authors:  C Mignon; F Parente; C Stavropoulou; P Collignon; A Moncla; C Turc-Carel; M G Mattei
Journal:  J Med Genet       Date:  1997-03       Impact factor: 6.318

2.  High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage.

Authors:  Nicholas J Wang; Dahai Liu; Alexander S Parokonny; N Carolyn Schanen
Journal:  Am J Hum Genet       Date:  2004-06-11       Impact factor: 11.025

3.  Infertility and marker chromosomes: application of molecular cytogenetic techniques in a case of inv dup(15).

Authors:  Tania M Vulcani-Freitas; Vera L Gil-da-Silva-Lopes; Marileila Varella-Garcia; Andréa T Maciel-Guerra
Journal:  J Appl Genet       Date:  2006       Impact factor: 3.240

4.  Characterization of an autism-associated segmental maternal heterodisomy of the chromosome 15q11-13 region.

Authors:  Dorota A Kwasnicka-Crawford; Wendy Roberts; Stephen W Scherer
Journal:  J Autism Dev Disord       Date:  2007-04

5.  The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications.

Authors:  G Floridia; M Piantanida; A Minelli; C Dellavecchia; C Bonaglia; E Rossi; G Gimelli; G Croci; F Franchi; S Gilgenkrantz; P Grammatico; L Dalprá; S Wood; C Danesino; O Zuffardi
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

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

Authors:  F L Long; D P Duckett; L J Billam; D K Williams; J A Crolla
Journal:  J Med Genet       Date:  1998-05       Impact factor: 6.318

7.  Large inv dup(15) chromosome in two generations.

Authors:  J J Van Der Smagt; J C Giltay; J J De Ne; G H Slabbers
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318

8.  Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26.

Authors:  M A Pujana; M Nadal; M Gratacòs; B Peral; K Csiszar; R González-Sarmiento; L Sumoy; X Estivill
Journal:  Genome Res       Date:  2001-01       Impact factor: 9.043

Review 9.  Angelman syndrome: etiology, clinical features, diagnosis, and management of symptoms.

Authors:  Renzo Guerrini; Romeo Carrozzo; Roberta Rinaldi; Paolo Bonanni
Journal:  Paediatr Drugs       Date:  2003       Impact factor: 3.022

10.  Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.

Authors:  S L Christian; W P Robinson; B Huang; A Mutirangura; M R Line; M Nakao; U Surti; A Chakravarti; D H Ledbetter
Journal:  Am J Hum Genet       Date:  1995-07       Impact factor: 11.025
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