Literature DB >> 7333027

Interstitial deletion 4q and Rieger syndrome.

I Ligutić, L Brecević, I Petković, T Kalogjera, Z Rajić.   

Abstract

Entities:  

Mesh：

Year:  1981        PMID： 7333027     DOI： 10.1111/j.1399-0004.1981.tb01042.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


× No keyword cloud information.
  14 in total

1.  Evidence that Rieger syndrome maps to 4q25 or 4q27.

Authors:  C Vaux; L Sheffield; C G Keith; L Voullaire
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

2.  A second locus for Rieger syndrome maps to chromosome 13q14.

Authors:  J C Phillips; E A del Bono; J L Haines; A M Pralea; J S Cohen; L J Greff; J L Wiggs
Journal:  Am J Hum Genet       Date:  1996-09       Impact factor: 11.025

3.  Multiple congenital anomalies including the Rieger eye malformation in a boy with interstitial deletion of (4) (q25-->q27) secondary to a balanced insertion in his normal father: evidence for haplotype insufficiency causing the Rieger malformation.

Authors:  A Schinzel; L Brecevic; F Dutly; A Baumer; F Binkert; R H Largo
Journal:  J Med Genet       Date:  1997-12       Impact factor: 6.318

4.  A new interstitial deletion of 4q (q21.1::q22.1).

Authors:  K Fagan; A Gill
Journal:  J Med Genet       Date:  1989-10       Impact factor: 6.318

5.  Pairwise linkage analysis of 11 loci on human chromosome 4.

Authors:  J C Murray; K H Buetow; M Smith; L Carlock; A Chakravarti; R F Ferrell; L Gedamu; C Gilliam; R Shiang; C R DeHaven
Journal:  Am J Hum Genet       Date:  1988-03       Impact factor: 11.025

Review 6.  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

7.  Closing in on the Rieger syndrome gene on 4q25: mapping translocation breakpoints within a 50-kb region.

Authors:  N A Datson; E Semina; A A van Staalduinen; H G Dauwerse; E J Meershoek; J J Heus; R R Frants; J T den Dunnen; J C Murray; G J van Ommen
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

8.  A new case of an interstitial deletion (4)(q25q27) characterised by molecular cytogenetic techniques and review of the literature.

Authors:  Sandra Anna Becker; Susanne Popp; Klaus Rager; Anna Jauch
Journal:  Eur J Pediatr       Date:  2003-02-19       Impact factor: 3.183

9.  Deletion of a single chromosome band 4q26 in a malformed girl: exclusion of Rieger syndrome associated gene(s) from the 4q26 segment.

Authors:  T Motegi; K Nakamura; T Terakawa; A Oohira; K Minoda; K Kishi; Y Yanagawa; H Hayakawa
Journal:  J Med Genet       Date:  1988-09       Impact factor: 6.318

10.  Genetic heterogeneity in Rieger eye malformation.

Authors:  E Legius; C E de Die-Smulders; F Verbraak; H Habex; R Decorte; P Marynen; J P Fryns; J J Cassiman
Journal:  J Med Genet       Date:  1994-04       Impact factor: 6.318
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.