Literature DB >> 1583648

Interstitial deletion of the distal long arm of chromosome 4.

P Sarda1, G Lefort, J P Fryns, C Humeau, D Rieu.   

Abstract

We report the first case of an interstitial deletion of the distal long arm of chromosome 4 (q31.22----q34.2). The major clinical features are described and compared to those of other published reports of del 4q, mainly those sharing a common deleted segment with the present case (both interstitial and terminal). This comparison suggests that the characteristic phenotype attributed to terminal deletions of 4q31----qter probably mainly results from loss of the segment q31----q33-34.

Mesh:

Year:  1992        PMID: 1583648      PMCID: PMC1015928          DOI: 10.1136/jmg.29.4.259

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


  4 in total

1.  Terminal deletion 4q in a severely retarded boy.

Authors:  M I de Michelena; P J Campos
Journal:  Am J Med Genet       Date:  1989-06

Review 2.  Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.

Authors:  A E Lin; K L Garver; G Diggans; M Clemens; S L Wenger; M W Steele; M C Jones; J Israel
Journal:  Am J Med Genet       Date:  1988-11

3.  Pericentric inversion and partial monosomy 4q associated with congenital anomalies.

Authors:  F Serville; A Broustet
Journal:  Hum Genet       Date:  1977-11-10       Impact factor: 4.132

4.  Interstitial deletion, del(4)(q33q35.1), in a mother and two children.

Authors:  M A Curtis; R A Smith; J Sibert; H E Hughes
Journal:  J Med Genet       Date:  1989-10       Impact factor: 6.318

  4 in total
  6 in total

1.  4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome.

Authors:  Goran Cuturilo; Björn Menten; Aleksandar Krstic; Danijela Drakulic; Ida Jovanovic; Vojislav Parezanovic; Milena Stevanovic
Journal:  Eur J Pediatr       Date:  2011-07-22       Impact factor: 3.183

2.  Interstitial 4q Deletion Syndrome Including NR3C2 Causing Pseudohypoaldosteronism.

Authors:  Amanda Barone Pritchard; Alyssa Ritter; Hutton M Kearney; Kosuke Izumi
Journal:  Mol Syndromol       Date:  2019-12-21

Review 3.  Toward the complete genomic map and molecular pathology of human chromosome 4.

Authors:  O Riess; B Winkelmann; J T Epplen
Journal:  Hum Genet       Date:  1994-07       Impact factor: 4.132

4.  Terminal 4q deletion syndrome.

Authors:  C M Kuldeep; A K Khare; Anubhav Garg; Asit Mittal; Lalit Gupta
Journal:  Indian J Dermatol       Date:  2012-05       Impact factor: 1.494

5.  Report of trisomy 2q34-qter and monosomy 4q35.2-qter in a child with mild dysmorphic syndrome and karyotype 46,XY,der(4)t(2;4)(q34;q35.2)pat.

Authors:  Juan Pablo Meza-Espinoza; Enrique Sáinz González; Christian J N León-León; Eliakym Arámbula-Meraz; José Alfredo Contreras-Gutiérrez; Noemí García-Magallanes; Jesús Madueña-Molina; Fred Luque-Ortega; Salvador Cervín-Serrano; Verónica Judith Picos-Cárdenas
Journal:  Mol Cytogenet       Date:  2020-05-19       Impact factor: 2.009

6.  Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array.

Authors:  Pingping Zhang; Yanmei Sun; Ping Huo; Haishen Tian; Jian Gao; Yali Li
Journal:  Mol Cytogenet       Date:  2020-04-10       Impact factor: 2.009

  6 in total

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