Literature DB >> 5902433

Familial de Lange syndrome with chromosome abnormalities.

A Falek, R Schmidt, G A Jervis.   

Abstract

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Mesh：

Year:  1966        PMID： 5902433

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  18 in total

1.  Familial translocation t(3p-;21q+) associated with both Down's and Sturge-Weber's syndrome in unbalanced state.

Authors:  M Habedank; G Kampe
Journal:  Humangenetik       Date:  1975-09-23

2.  Tetralogy of fallot and congenital connection between the left subclavian artery and the pulmonary artery: possible relationship to a congenital left-hand deformity.

Authors:  J T Bricker; M R Nihill; D G McNamara
Journal:  Tex Heart Inst J       Date:  1984-03

3.  Cornelia de Lange syndrome with ring chromosome 3.

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

4.  Partial trisomy 3q.

Authors:  E Yunis; L Quintero; A Casteñeda; E Ramirez; M Leibovici
Journal:  Hum Genet       Date:  1979-05-10       Impact factor: 4.132

5.  An unusual chromosomal segregation in a family with a translocation between chromosomes 3 and 12.

Authors:  S Sachdeva; G F Smith; P Justice
Journal:  J Med Genet       Date:  1974-09       Impact factor: 6.318

6.  Double chromosomal aberration. Trisomy G and the balanced translocation t(3p--;17q+).

Authors:  I Subrt; H Prchliková
Journal:  Humangenetik       Date:  1969-10

7.  De Lange syndrome: report of 20 cases.

Authors:  R G McArthur; J H Edwards
Journal:  Can Med Assoc J       Date:  1967-04-29       Impact factor: 8.262

8.  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

9.  Chromosome banding study of the Cornelia De Lange syndrome.

Authors:  J R Merikangas; K Merikangas; L Katz; S Pan
Journal:  Hum Genet       Date:  1977-11-10       Impact factor: 4.132

10.  Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 --> qter) detected in an autistic boy.

Authors:  Isabel M Carreira; Joana B Melo; Carlos Rodrigues; Liesbeth Backx; Joris Vermeesch; Anja Weise; Nadezda Kosyakova; Guiomar Oliveira; Eunice Matoso
Journal:  Mol Cytogenet       Date:  2009-08-04       Impact factor: 2.009
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