Literature DB >> 627107

Serial duplication of 10 (q11 leads to q22) in a patient with minor congenital malformations.

W Vogel, E Back, W Imm.   

Abstract

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Year:  1978        PMID： 627107

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  11 in total

1.  A new case of proximal 10q partial trisomy.

Authors:  M I de Michelena; P J Campos
Journal:  J Med Genet       Date:  1991-03       Impact factor: 6.318

2.  Duplication 17q mosaicism: an infant with features of Ellis-van Creveld syndrome.

Authors:  A Serotkin; J Stamberg; L Waber
Journal:  J Med Genet       Date:  1988-04       Impact factor: 6.318

3.  Partial distal 10q trisomy due to de novo amplification: A new case without furrows or ridges in fingers and palms.

Authors:  Aliakbar Rahbarimanesh; Pupak Derakhshandeh-Peykar; Amirhassan Barkhordari; Reza Ebrahimzadeh-Vesal; Soja Shamizadeh Kalkhoran
Journal:  Rep Biochem Mol Biol       Date:  2013-04

4.  Partial duplication of the short arm of chromosome 10. Karyotype: 46,XX,dup(10p)(pter to p12::p12::p12 to qter).

Authors:  J P Fryns; J Deroover; J Haegeman; H Van den Berghe
Journal:  Hum Genet       Date:  1979-03-12       Impact factor: 4.132

5.  Tandem duplication (5q13 to 22) in a mentally deficient girl.

Authors:  E Kessel; R A Pfeiffer
Journal:  Hum Genet       Date:  1979-11       Impact factor: 4.132

6.  Serial duplication of 10 (q21 to q22) in a mentally retarded boy with congenital malformations.

Authors:  M Koivisto; R Herva; S L Linna
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

7.  The use of array-CGH in a cohort of Greek children with developmental delay.

Authors:  Emmanouil Manolakos; Annalisa Vetro; Konstantinos Kefalas; Stamatia-Maria Rapti; Eirini Louizou; Antonios Garas; George Kitsos; Lefteris Vasileiadis; Panagiota Tsoplou; Makarios Eleftheriades; Panagiotis Peitsidis; Sandro Orru; Thomas Liehr; Michael B Petersen; Loretta Thomaidis
Journal:  Mol Cytogenet       Date:  2010-11-09       Impact factor: 2.009

8.  Further delineation of the partial proximal trisomy 10q syndrome.

Authors:  C M Aalfs; J M Hoovers; M A Nieste-Otter; M M Mannens; R C Hennekam; N J Leschot
Journal:  J Med Genet       Date:  1995-12       Impact factor: 6.318

9.  Partial duplication of the short arm of chromosome 9 (p13 leads to p22) in a child with typical 9p trisomy phenotype.

Authors:  J P Fryns; P Casaer; H Van den Berghe
Journal:  Hum Genet       Date:  1979-01-25       Impact factor: 4.132

10.  Confirmation of a de novo duplication, dup(10)(q24 leads to q26), by GOT1 gene dosage studies.

Authors:  D J Tomkins; B J Gitelman; M H Roberts
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132
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