Literature DB >> 14242103

[17-18 RING-CHROMOSOMES AND CONGENITAL MALFORMATIONS IN A YOUNG GIRL].

J DE GROUCHY, B LEVEQUE, C DEBAUCHEZ, C SALMON, M LAMY, J MARIE.   

Abstract

Entities:  

Keywords:  BLOOD GROUPS; CHILD; CHROMOSOME ABNORMALITIES; DERMATOGLYPHICS; DIAGNOSIS, LABORATORY

Mesh：

Substances：

Year:  1964        PMID： 14242103

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  8 in total

Review 1.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

Authors:  J Kunze; E Stephan; M Tolksdorf
Journal:  Humangenetik       Date:  1972

Review 2.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

Authors:  I W Lurie; G I Lazjuk
Journal:  Humangenetik       Date:  1972

Review 3.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23

4.  Comparative behavior of ring chromosomes.

Authors:  M L Kistenmacher; H H Punnett
Journal:  Am J Hum Genet       Date:  1970-05       Impact factor: 11.025

5.  On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment.

Authors:  K Bender; K Burckhardt
Journal:  Humangenetik       Date:  1970

6.  An unstable ring chromosome in a female infant with hypotonia, seizures, and retarded development.

Authors:  L Atkins; R T Sceery; M E Keenan
Journal:  J Med Genet       Date:  1966-06       Impact factor: 6.318

7.  Prenatal diagnosis in a mentally retarded woman with mosaic ring chromosome 18.

Authors:  Eiman Bagherizadeh; Farkhondeh Behjati; Seyed Hoseinali Saberi; Yousef Shafeghati
Journal:  Indian J Hum Genet       Date:  2011-05

8.  Breakpoints and deleted genes identification of ring chromosome 18 in a Chinese girl by whole-genome low-coverage sequencing: a case report study.

Authors:  Hui Yao; Chuanchun Yang; Xiaoli Huang; Luhong Yang; Wei Zhao; Dan Yin; Yuan Qin; Feng Mu; Lin Liu; Ping Tian; Zhisheng Liu; Yun Yang
Journal:  BMC Med Genet       Date:  2016-07-22       Impact factor: 2.103
  8 in total

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