Literature DB >> 712481

The association of chromosome 3 duplication and the Cornelia de Lange syndrome.

G N Wilson, V C Hieber, R D Schmickel.   

Abstract

Two unrelated children with features of the Cornelia de Lange syndrome, including mental retardation, growth retardation, glaucoma, and a similar facies, had duplications corresponding to bands q25 leads to q29 of chromosome 3. These patients were compared to others with duplications of chromosome 3 and to a large series of patients with Cornelia de Lange syndrome. Diseases that sometimes involve characteristic chromosomal changes but have normal chromosomes in other instances are discussed.

Entities:  

Mesh:

Substances:

Year:  1978        PMID: 712481     DOI: 10.1016/s0022-3476(78)81077-4

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  12 in total

1.  Cornelia de Lange syndrome with ring chromosome 3.

Authors:  G N Wilson
Journal:  J Med Genet       Date:  1991-02       Impact factor: 6.318

2.  Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting.

Authors:  S Goobie; J Knijnenburg; D Fitzpatrick; F H Sharkey; A C Lionel; C R Marshall; T Azam; M Shago; K Chong; R Mendoza-Londono; N S den Hollander; C Ruivenkamp; E Maher; H J Tanke; K Szuhai; R F Wintle; S W Scherer
Journal:  Cytogenet Genome Res       Date:  2009-03-11       Impact factor: 1.636

Review 3.  Partial 3q duplication syndrome and assignment of D3S5 to 3q25-3q28.

Authors:  A J van Essen; K Kok; A van den Berg; B de Jong; F Stellink; A F Bos; H Scheffer; C H Buys
Journal:  Hum Genet       Date:  1991-06       Impact factor: 4.132

4.  Partial trisomy 3q causing mild Cornelia de Lange phenotype.

Authors:  S E Holder; L M Grimsley; R W Palmer; L J Butler; M Baraitser
Journal:  J Med Genet       Date:  1994-02       Impact factor: 6.318

Review 5.  Chromosome rearrangements in cornelia de Lange syndrome (CdLS): report of a der(3)t(3;12)(p25.3;p13.3) in two half sibs with features of CdLS and review of reported CdLS cases with chromosome rearrangements.

Authors:  Cheryl DeScipio; Maninder Kaur; Dinah Yaeger; Jeffrey W Innis; Nancy B Spinner; Laird G Jackson; Ian D Krantz
Journal:  Am J Med Genet A       Date:  2005-09-01       Impact factor: 2.802

6.  A Pure 2-Mb 3q26.2 Duplication Proximal to the Critical Region of 3q Duplication Syndrome.

Authors:  Miriam Coelho Molck; Milena Simioni; Társis Paiva Vieira; Fabíola Paoli Monteiro; Vera L Gil-da-Silva-Lopes
Journal:  Mol Syndromol       Date:  2018-06-08

7.  Cornelia de lange syndrome.

Authors:  Naeimeh Tayebi
Journal:  Indian J Hum Genet       Date:  2008-01

Review 8.  Cohesin and human disease.

Authors:  Jinglan Liu; Ian D Krantz
Journal:  Annu Rev Genomics Hum Genet       Date:  2008       Impact factor: 8.929

9.  Chromosomes in the Cornelia de Lange syndrome.

Authors:  B Beck; M Mikkelsen
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

10.  Clinical, Cytogenetic, and Biochemical Analyses of a Family with a t(3;13)(q26.2;p11.2): Further Delineation of 3q Duplication Syndrome.

Authors:  M Abreu-González; C García-Delgado; A Cervantes; A Aparicio-Onofre; R Guevara-Yáñez; R Sánchez-Urbina; M P Gallegos-Arreola; A Luna-Angulo; F J Estrada; V F Morán-Barroso
Journal:  Case Rep Genet       Date:  2013-09-18
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.