Literature DB >> 1684563

Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type.

A A Bergen1, C Samanns, E J Schuurman, L van Osch, D B van Dorp, A J Pinckers, E Bakker, A Gal, G J van Ommen, E M Bleeker-Wagemakers.   

Abstract

An extensive linkage analysis was performed by studying ten Xp22 loci in ten families segregating for X-linked ocular albinism of the Nettleship-Falls type (XOA). Linkage was confirmed between the XOA locus (OA1) and both DXS16 (theta max = 0.10, zeta max = 4.09) and DXS237 (theta max = 0.12, zeta max = 2.53). Linkage was found between OA1 and the loci DXS85 (theta max = 0.00, zeta max = zeta max = 4.37), DXS143 (theta max = 0.04, zeta max = 3.74), STS (theta max = 0.05, zeta max = 2.48), DXF30S1 (DXS278) (theta max = 0.07, zeta max = 8.79) and DXF30S2/3 (DXS278) (theta max = 0.00, zeta max = 14.93). An indication for linkage was found between OA1 and the loci DXS43 (theta max = 0.10, zeta max = 1.58) and DXS31 (theta max = 0.12, zeta max = 1.55). The analysis of multiple informative meioses suggests the order Xpter-(DXS31, DXS89)-(DXF30S1, DXS237)-(DXF30S2/3, OA1)-DXS143-(DXS16, DXS43)-Xcen. Various multipoint linkage analyses using the DNA loci order DXF30S1-STS-DXS237-DXS143-DXS16 significantly favour the position of OA1 between DXS237 and DXS143. These results further determine the genetic map around the XOA locus on the distal Xp and may be useful for DNA diagnosis in families with XOA.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1684563     DOI: 10.1007/bf00206065

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  25 in total

Review 1.  Report of the committee on the genetic constitution of the X chromosome.

Authors:  K E Davies; J L Mandel; A P Monaco; R L Nussbaum; H F Willard
Journal:  Cytogenet Cell Genet       Date:  1990

2.  An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry.

Authors:  R E Schnur; B J Trask; G van den Engh; H H Punnett; M Kistenmacher; M A Tomeo; R E Naids; R L Nussbaum
Journal:  Am J Hum Genet       Date:  1989-11       Impact factor: 11.025

3.  Long-range restriction map of the terminal part of the short arm of the human X chromosome.

Authors:  C Petit; J Levilliers; J Weissenbach
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

4.  Report of the committee on linkage and gene order.

Authors:  B Keats; J Ott; M Conneally
Journal:  Cytogenet Cell Genet       Date:  1989

5.  BclI RFLP at the DXS16 locus.

Authors:  B de Martinville; N A Uhrhammer
Journal:  Nucleic Acids Res       Date:  1988-11-25       Impact factor: 16.971

6.  A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm.

Authors:  M Koenig; G Camerino; R Heilig; J L Mandel
Journal:  Nucleic Acids Res       Date:  1984-05-25       Impact factor: 16.971

7.  X/Y translocation in a family with X-linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogene.

Authors:  A Ballabio; G Parenti; R Carrozzo; G Coppa; L Felici; V Migliori; M Silengo; P Franceschini; G Andria
Journal:  Clin Genet       Date:  1988-07       Impact factor: 4.438

8.  Linkage relationships of X-linked choroideremia to DXYS1 and DXS3.

Authors:  I M MacDonald; R M Sandre; P Wong; A G Hunter; M P Tenniswood
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

9.  Partial deletions of a sequence family ("DXS278") and its physical linkage to steroid sulfatase as detected by pulsed-field gel electrophoresis.

Authors:  R E Schnur; R G Knowlton; M A Musarella; M Muenke; R L Nussbaum
Journal:  Genomics       Date:  1990-10       Impact factor: 5.736

10.  Choroideremia-locus maps between DXS3 and DXS11 on Xq.

Authors:  A Gal; F Brunsmann; D Hogenkamp; K Rüther; D Ahlert; T F Wienker; W Hammerstein; I H Pawlowitzki
Journal:  Hum Genet       Date:  1986-06       Impact factor: 4.132

View more
  13 in total

Review 1.  Albinism: modern molecular diagnosis.

Authors:  S M Carden; R E Boissy; P J Schoettker; W V Good
Journal:  Br J Ophthalmol       Date:  1998-02       Impact factor: 4.638

2.  A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosome.

Authors:  J J Assink; N T Tijmes; J B ten Brink; R J Oostra; F C Riemslag; P T de Jong; A A Bergen
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

3.  Localization of a novel X-linked progressive cone dystrophy gene to Xq27: evidence for genetic heterogeneity.

Authors:  A A Bergen; A J Pinckers
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

4.  Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1.

Authors:  A A Bergen; J B ten Brink; F Riemslag; E J Schuurman; F Meire; N Tijmes; P T de Jong
Journal:  J Med Genet       Date:  1996-10       Impact factor: 6.318

5.  Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism.

Authors:  A Meindl; D Hosenfeld; W Brückl; S Schuffenhauer; J Jenderny; A Bacskulin; H C Oppermann; O Swensson; P Bouloux; T Meitinger
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

6.  Refinement of the chromosomal position of the X linked juvenile retinoschisis gene.

Authors:  A A Bergen; J B ten Brink; L M Bleeker-Wagemakers; M J van Schooneveld
Journal:  J Med Genet       Date:  1994-12       Impact factor: 6.318

7.  Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOB.

Authors:  A A Bergen; P Kestelyn; M Leys; F Meire
Journal:  J Med Genet       Date:  1994-07       Impact factor: 6.318

8.  Vision in albinism.

Authors:  C G Summers
Journal:  Trans Am Ophthalmol Soc       Date:  1996

9.  Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

Authors:  Y Zhang; R McMahon; S J Charles; J S Green; A T Moore; D E Barton; J R Yates
Journal:  J Med Genet       Date:  1993-11       Impact factor: 6.318

10.  X linked progressive cone dystrophy. Localisation of the gene locus to Xp21-p11.1 by linkage analysis.

Authors:  F M Meire; A A Bergen; A De Rouck; M Leys; J W Delleman
Journal:  Br J Ophthalmol       Date:  1994-02       Impact factor: 4.638

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.