Literature DB >> 669716

Partial deletion 10q.

R C Lewandowski, M K Kukolich, J W Sears, C B Mankinen.   

Abstract

The patient described represents the first reported case of partial deletion 10q. The patient is compared to the partial trisomy 10q syndrome.

Entities:  

Mesh：

Year:  1978        PMID： 669716     DOI： 10.1007/BF00291317

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  3 in total

1.  New chromosomal syndromes.

Authors:  R C Lewandowski; J J Yunis
Journal:  Am J Dis Child       Date:  1975-04

2.  A new syndrome resulting from partial trisomy for the distal third of the long arm of chromosome 10.

Authors:  J J Yunis; O Sanchez
Journal:  J Pediatr       Date:  1974-04       Impact factor: 4.406

3.  The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability.

Authors:  T Caspersson; G Lomakka; L Zech
Journal:  Hereditas       Date:  1972       Impact factor: 3.271
  3 in total
  10 in total

1.  Terminal deletion of the long arm of chromosome 10.

Authors:  H Curtis; R T Howell; C Cope
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

2.  Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).

Authors:  J Brusnický; K M van Heerden; G de Jong; A S Cronjé; A E Retief
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

3.  A case of interstitial deletion of 10q25.2----q26.1.

Authors:  D E Rooney; K Williams; D V Coleman; A Habel
Journal:  J Med Genet       Date:  1989-01       Impact factor: 6.318

4.  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

5.  Diagnostic Value of Microarray Method in Autism Spectrum Disorder, Intellectual Disability, and Multiple Congenital Anomalies and Some Candidate Genes for Autism: Experience of Two Centers.

Authors:  Akif Ayaz; Alper Gezdirici; Elif Yilmaz Gulec; Ozge Ozalp; Abdullah Huseyin Koseoglu; Zeynep Dogru; Sinem Yalcintepe
Journal:  Medeni Med J       Date:  2022-06-23

6.  Monosomy 10qter.

Authors:  C Turleau; J de Grouchy; G Ponsot; D Bouygues
Journal:  Hum Genet       Date:  1979-04-05       Impact factor: 4.132

7.  Mild Phenotype in a Patient with a De Novo 6.3 Mb Distal Deletion at 10q26.2q26.3.

Authors:  George A Tanteles; Elpiniki Nikolaou; Yiolanda Christou; Angelos Alexandrou; Paola Evangelidou; Violetta Christophidou-Anastasiadou; Carolina Sismani; Savvas S Papacostas
Journal:  Case Rep Genet       Date:  2015-07-29

Review 8.  Chromosome 10q26 deletion syndrome: Two new cases and a review of the literature.

Authors:  Shaobin Lin; Yi Zhou; Qun Fang; Jianzhu Wu; Zhiqiang Zhang; Yuanjun Ji; Yanmin Luo
Journal:  Mol Med Rep       Date:  2016-10-19       Impact factor: 2.952

9.  Headbobber: a combined morphogenetic and cochleosaccular mouse model to study 10qter deletions in human deafness.

Authors:  Annalisa Buniello; Rachel E Hardisty-Hughes; Johanna C Pass; Eva Bober; Richard J Smith; Karen P Steel
Journal:  PLoS One       Date:  2013-02-14       Impact factor: 3.240

Review 10.  A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature.

Authors:  Roxana Popescu; Mihaela Grămescu; Lavinia Caba; Monica-Cristina Pânzaru; Lăcrămioara Butnariu; Elena Braha; Setalia Popa; Cristina Rusu; Georgeta Cardos; Monica Zeleniuc; Violeta Martiniuc; Cristina Gug; Luminiţa Păduraru; Maria Stamatin; Carmen C Diaconu; Eusebiu Vlad Gorduza
Journal:  Genes (Basel)       Date:  2021-12-07       Impact factor: 4.096
  10 in total

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