Literature DB >> 6517095

Del(15)(q22q24) syndrome with Potter sequence.

R D Clark.   

Abstract

Mesh：

Year:  1984        PMID： 6517095     DOI： 10.1002/ajmg.1320190409

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  7 in total

1.  Deletion 15q21.1----q22.1 resulting from a paternal insertion into chromosome 5.

Authors:  M Y Yip; M Selikowitz; N Don; A Kovacic; S Purvis-Smith; P R Lam-Po-Tang
Journal:  J Med Genet       Date:  1987-11       Impact factor: 6.318

2.  Interstitial deletion of chromosome 15: two cases.

Authors:  L D Formiga; L Poenaru; F Couronne; E Flori; J L Eibel; M M Deminatti; J B Savary; J L Lai; S Gilgenkrantz; M Pierson
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

3.  An infant with deletion of the distal long arm of chromosome 15 (q26.1----qter) and loss of insulin-like growth factor 1 receptor gene.

Authors:  E W Roback; A J Barakat; V G Dev; M Mbikay; M Chrétien; M G Butler
Journal:  Am J Med Genet       Date:  1991-01

4.  Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping.

Authors:  Ayman W El-Hattab; Teresa A Smolarek; Martha E Walker; Elizabeth K Schorry; LaDonna L Immken; Gayle Patel; Mary-Alice Abbott; Brendan C Lanpher; Zhishuo Ou; Sung-Hae L Kang; Ankita Patel; Fernando Scaglia; James R Lupski; Sau Wai Cheung; Pawel Stankiewicz
Journal:  Hum Genet       Date:  2009-06-26       Impact factor: 4.132

Review 5.  Coexistence of urogenital malformations in a female fetus with de novo 15q24 microdeletion and a literature review.

Authors:  Yaobin Liu; Beth Mapow
Journal:  Mol Genet Genomic Med       Date:  2020-05-13       Impact factor: 2.183

6.  A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH.

Authors:  Eva Klopocki; Luitgard M Graul-Neumann; Ulrike Grieben; Holger Tönnies; Hans-Hilger Ropers; Denise Horn; Stefan Mundlos; Reinhard Ullmann
Journal:  Eur J Pediatr       Date:  2007-10-12       Impact factor: 3.183

7.  De novo interstitial deletion of 15q22q23 with global developmental delay and hypotonia: the first Korean case.

Authors:  Ha-Su Kim; Jin-Yeong Han; Myo-Jing Kim
Journal:  Korean J Pediatr       Date:  2015-08-21
  7 in total

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