Literature DB >> 5539084

Clinical and chromosomal studies of the 18q- syndrome.

W Wertelecki, P S Gerald.   

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Year:  1971        PMID： 5539084     DOI： 10.1016/s0022-3476(71)80262-7

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


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  26 in total

1.  Adult-onset seizure disorder in the 18q deletion syndrome.

Authors:  N Adab; A J Larner
Journal:  J Neurol       Date:  2006-03-20       Impact factor: 4.849

2.  Growth hormone deficiency in children with chromosomal abnormalities.

Authors:  H P Schwarz; S C Duck
Journal:  Arch Dis Child       Date:  1990-03       Impact factor: 3.791

3.  Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1.

Authors:  Soraya Beiraghi; Swapan K Nath; Matthew Gaines; Desh D Mandhyan; David Hutchings; Uppala Ratnamala; Ken McElreavey; Lucia Bartoloni; Gregory S Antonarakis; Stylianos E Antonarakis; Uppala Radhakrishna
Journal:  Am J Hum Genet       Date:  2007-05-18       Impact factor: 11.025

4.  A case of (13q;18q) translocation with proximal 13q monosomy.

Authors:  Y Suzuki; K Ono; S Oka; T Matsubara; M Arima; Y Nakagome
Journal:  Hum Genet       Date:  1977-10-14       Impact factor: 4.132

5.  Molecular characterization of patients with 18q23 deletions.

Authors:  G Strathdee; R Sutherland; J J Jonsson; R Sataloff; M Kohonen-Corish; D Grady; J Overhauser
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

Review 6.  Pericentric inversions. Problems and significance for clinical genetics.

Authors:  P Kaiser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  Structural aberrations of chromosome 18. II. The 18q- syndrome. Report of three cases.

Authors:  A Schinzel; K Hayashi; W Schmid
Journal:  Humangenetik       Date:  1975

8.  Craniofacial and Neurological Phenotype in a Patient with De Novo 18q Microdeletion and 18p Microduplication.

Authors:  Christos Yapijakis; Antonia Angelopoulou; Emmanuel Manolakos; Costas Voumvourakis
Journal:  Adv Exp Med Biol       Date:  2020       Impact factor: 2.622

9.  Interstitial deletions are not the main mechanism leading to 18q deletions.

Authors:  G Strathdee; W Harrison; H C Riethman; S A Goodart; J Overhauser
Journal:  Am J Hum Genet       Date:  1994-06       Impact factor: 11.025

10.  Case report of de novo dup(18p)/del(18q) and r(18) mosaicism.

Authors:  Enkhtuvshin Gereltzul; Yoshiyuki Baba; Naoto Suda; Momotoshi Shiga; Maristela Sayuri Inoue; Michiko Tsuji; Insik Shin; Yukio Hirata; Kimie Ohyama; Keiji Moriyama
Journal:  J Hum Genet       Date:  2008-08-05       Impact factor: 3.172
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