Clinical Genetics

Volume 55, Number 2, February 1999

Links for this Journal

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002
Ingenta Connect ISSN
Open URL

Mini Review

Glaucoma genetics, present and future
pp. 71-79(9)
Authors: Friedman, James S; Walter, Michael A

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http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00001
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=71&epage=79
http://dx.doi.org/10.1034/j.1399-0004.1999.550201.x

HotSpots

Fetal gene therapy - a focus on prevention versus convention.
pp. 80-80(1)
Author: Lewis, Me Suzanne

Links for this article

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00002
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=80&epage=80
http://dx.doi.org/10.1034/j.1399-0004.1999.550202.x

Intra-amniotic viral gene transfer highlights the potential for in utero molecular therapies
pp. 80-81(2)
Author: Lewis, Me Suzanne

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http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00003
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=80&epage=81
http://dx.doi.org/10.1034/j.1399-0004.1999.550202-1.x

Original Articles

The tools of gene therapy can create new insights in developmental biology
pp. 81-82(2)
Author: Lewis, Me Suzanne

Links for this article

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00004
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=81&epage=82
http://dx.doi.org/10.1034/j.1399-0004.1999.550202-2.x

Fetal gene therapy confers stable gene expression, germline and widespread somatic cell transfection
pp. 82-84(3)
Author: Lewis, Me Suzanne

Links for this article

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00005
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=82&epage=84
http://dx.doi.org/10.1034/j.1399-0004.1999.550202-3.x

Genetic landmarks through philately - porphyria and its effect on world history
pp. 85-87(3)
Authors: Chudley, Albert E; Haworth, James C

Links for this article

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00006
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=85&epage=87
http://dx.doi.org/10.1034/j.1399-0004.1999.550203.x

Evaluation of the facioscapulohumeral muscular dystrophy (FSHD1) phenotype in correlation to the concurrence of 4q35 and 10q26 fragments
pp. 88-94(7)
Authors: Köhler, Jutta; Röhrig, Dorothee; Bathke, Klaus D; Koch, Manuela C

Links for this article

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00007
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=88&epage=94
http://dx.doi.org/10.1034/j.1399-0004.1999.550204.x

Pattern of central nervous system anomalies in a population with a high rate of consanguineous marriages
pp. 95-102(8)
Authors: Al-Gazali, Li; Sztriha, L; Dawodu, A; Bakir, M; Varghese, M; Varady, E; Scorer, J; Abdulrazzaq, Ym; Bener, A; Padmanabhan, R

Links for this article

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00008
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=95&epage=102
http://dx.doi.org/10.1034/j.1399-0004.1999.550205.x

Antibody deficiency, growth retardation, spondyloepiphyseal dysplasia and retinal dystrophy: a novel syndrome
pp. 103-109(7)
Author: Roifman, Chaim M

Links for this article

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00009
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=103&epage=109
http://dx.doi.org/10.1034/j.1399-0004.1999.550206.x

Novel exon skipping mutation in the fibrillin-1 gene: Two `hot spots' for the neonatal Marfan syndrome
pp. 110-117(8)
Authors: Booms, Patrick; Cisler, Jason; Mathews, Kurt R.; Godfrey, Maurice; Tiecke, Frank; Kaufmann, Ursula C.; Vetter, Ulrich; Hagemeier, Christian; Robinson, Peter N.

Links for this article

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00010
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=110&epage=117
http://dx.doi.org/10.1034/j.1399-0004.1999.550207.x

Short Reports

Alternative splicing of exon 37 of FBN1 deletes part of an `eight-cysteine' domain resulting in the Marfan syndrome
pp. 118-121(4)
Authors: McGrory, Joel; Cole, William G

Links for this article

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00011
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=118&epage=121
http://dx.doi.org/10.1034/j.1399-0004.1999.550208.x

Centromere-telomere (12;8p) fusion, telomeric 12q translocation, and i(12p) trisomy
pp. 122-126(5)
Authors: Rivera, Horacio; Vásquez, Ana Isabel; Perea, Francisco J

Links for this article

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00012
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=122&epage=126
http://dx.doi.org/10.1034/j.1399-0004.1999.550209.x

Letters to the Editor

Deletion of chromosome 4p detected by FISH in a girl with normal high resolution karyotype
pp. 127-129(3)

Links for this article

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00013
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=127&epage=129
http://dx.doi.org/10.1034/j.1399-0004.1999.550210.x

Mutations associated with very late-onset metachromatic leukodystrophy
pp. 130-130(1)

Links for this article

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00014
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=130&epage=130
http://dx.doi.org/10.1034/j.1399-0004.1999.550211.x

Preaxial polydactyly in an infant with Down's syndrome
pp. 131-132(2)

Links for this article

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00015
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=131&epage=132
http://dx.doi.org/10.1034/j.1399-0004.1999.550212.x

Original Article

Correspondence
pp. 133-134(2)

Links for this article

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00016
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=133&epage=134
http://dx.doi.org/10.1034/j.1399-0004.1999.550213.x

Articles

Obituary
pp. 135-136(2)

Links for this article

http://www.ingentaconnect.com/content/mksg/cge/1999/00000055/00000002/art00017
http://openurl.ingenta.com/content?genre=article&issn=0009-9163&volume=55&issue=2&spage=135&epage=136
http://dx.doi.org/10.1034/j.1399-0004.1999.550214.x