Literature DB >> 2880102

RFLP for linkage analysis of fragile X syndrome.

W T Brown, Y Wu, A C Gross, C B Chan, C S Dobkin, E C Jenkins.   

Abstract

Entities:  

Mesh：

Year:  1987        PMID： 2880102     DOI： 10.1016/s0140-6736(87)90103-6

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


× No keyword cloud information.
  13 in total

1.  Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.

Authors:  M Schmidt; A Certoma; D Du Sart; P Kalitsis; M Leversha; K Fowler; L Sheffield; I Jack; D M Danks
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

2.  Genetic mapping of two new DNA markers in Xq26-q28 relative to the fragile-X syndrome locus.

Authors:  R Sood; L M Mulligan; R Poon; B N White; J J Holden
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

3.  Physical mapping of DXS134 close to the DXS52 locus.

Authors:  M V Bell; M N Patterson; H R Dorkins; K E Davies
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

4.  Molecular studies of haemophilia B in Sweden. Identification of patients with total deletion of the factor IX gene and without inhibitory antibodies.

Authors:  C Wadelius; M Blombäck; U Pettersson
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

5.  In situ hybridization studies using a molecular probe that maps to Xq27-Zq28.

Authors:  A M Duncan; C Morgan
Journal:  Hum Genet       Date:  1990-04       Impact factor: 4.132

6.  Multilocus analysis of the fragile X syndrome.

Authors:  W T Brown; A Gross; C Chan; E C Jenkins; J L Mandel; I Oberlé; B Arveiler; G Novelli; S Thibodeau; R Hagerman
Journal:  Hum Genet       Date:  1988-03       Impact factor: 4.132

7.  Linkage studies in a large fragile X family.

Authors:  M Patterson; M Bell; W Kress; K E Davies; U Froster-Iskenius
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

8.  Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families.

Authors:  B Arveiler; I Oberlé; A Vincent; M H Hofker; P L Pearson; J L Mandel
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

9.  Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome.

Authors:  G K Suthers; J C Mulley; M A Voelckel; N Dahl; M L Väisänen; P Steinbach; I A Glass; C E Schwartz; B A van Oost; S N Thibodeau
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

10.  Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome.

Authors:  S N Thibodeau; H R Dorkins; K R Faulk; R Berry; A C Smith; R Hagerman; A King; K E Davies
Journal:  Hum Genet       Date:  1988-07       Impact factor: 4.132
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.