Anmelden/Registrieren
Erscheinungsjahr:
 
Zurück zur geteilten Ansicht
Alfons Meindl

Veröffentlichungen von Alfons Meindl zu Meindl, Alfons ->
weitere Veröffentlichungen von Alfons Meindl:
HUGO meeting in Toronto, March 1997 Calm before the storm (1997)
A patient with an interstitial deletion in Xp22.3 locates the gene for X-linked recessive chondrodysplasia punctata to within a one megabase interval (1994)
Molecular modelling of the Norrie disease protein predicts a cystine knot growth factor tertiary structure (1993)
Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1 (2000)
Norrie disease is caused by mutations in an extracellular protein resembling C–terminal globular domain of mucins (1992)
Mutations in a Δ87 sterolisomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata (1999)
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa (2000)
Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism (1994)
An L-type calcium-channel gene mutated in incomplete X-linked congenitalstationary night blindness (1998)
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein (2000)
SCA2 trinucleotide expansion in German SCA patients (1997)
Host response to EBV infection in X-linked lymphoproliferative diseaseresults from mutations in an SH2-domain encoding gene (1998)
The DNA sequence of the human X chromosome (2005)
Veröffentlichungen zu Meindl, Alfons
Zurück zur geteilten Ansicht
Verfasser Titel Jahr absteigend sortierenaufsteigend sortieren
zeige Details
1
Meindl, Alfons HUGO meeting in Toronto, March 1997 Calm before the storm
in: Journal of molecular medicine , ISSN 1432-1440, Vol. 75 (10. 1997), p. 762-764
Zugang: zum Volltext
ähnliche Vorschläge
1997
zeige Details
2
Klink, Albrecht, Meindl, Alfons, ... A patient with an interstitial deletion in Xp22.3 locates the gene for X-linked recessive chondrodysplasia punctata to within a one megabase interval
in: Human genetics , ISSN 1432-1203, Vol. 93 (4. 1994), p. 463-466
Zugang: zum Volltext
ähnliche Vorschläge
1994
zeige Details
3
Meitinger, Thomas, Meindl, Alfons, ... Molecular modelling of the Norrie disease protein predicts a cystine knot growth factor tertiary structure
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 5, No. 4 (1993), p. 376-380
Zugang: zum Volltext
ähnliche Vorschläge
1993
zeige Details
4
Jacobi, Felix K., Broghammer, Martina, ... Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1
in: Human genetics , ISSN 1432-1203, Vol. 107 (1. 2000), p. 89-91
Zugang: zum Volltext
ähnliche Vorschläge
2000
zeige Details
5
Meindl, Alfons, Berger, Wolfgang, ... Norrie disease is caused by mutations in an extracellular protein resembling C–terminal globular domain of mucins
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 2, No. 2 (1992), p. 139-143
Zugang: zum Volltext
ähnliche Vorschläge
1992
zeige Details
6
Derry, Jonathan M.J., Gormally, Emmanuelle, ... Mutations in a Δ<sup>8</sup>-Δ<sup>7</sup> sterolisomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 22, No. 3 (1999), p. 286-290
Zugang: zum Volltext
ähnliche Vorschläge
1999
zeige Details
7
Vervoort, Raf, Lennon, Alan, ... Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 25, No. 4 (2000), p. 462-466
Zugang: zum Volltext
ähnliche Vorschläge
2000
zeige Details
8
Muscatelli, Françoise, Strom, Tim M., ... Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 372, No. 6507 (1994), p. 672-676
Zugang: zum Volltext
ähnliche Vorschläge
1994
zeige Details
9
Strom, Tim M., Nyakatura, Gerald, ... An L-type calcium-channel gene mutated in incomplete X-linked congenitalstationary night blindness
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 19, No. 3 (1998), p. 260-263
Zugang: zum Volltext
ähnliche Vorschläge
1998
zeige Details
10
Pusch, Carsten M., Zeitz, Christina, ... The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 26, No. 3 (2000), p. 324-327
Zugang: zum Volltext
ähnliche Vorschläge
2000
zeige Details
11
Riess, Olaf, Laccone, Franco A., ... SCA2 trinucleotide expansion in German SCA patients
in: Neurogenetics , ISSN 1364-6753, Vol. 1 (1. 1997), p. 59-64
Zugang: zum Volltext
ähnliche Vorschläge
1997
zeige Details
12
Coffey, Alison J., Brooksbank, Robert A., ... Host response to EBV infection in X-linked lymphoproliferative diseaseresults from mutations in an SH2-domain encoding gene
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 20, No. 2 (1998), p. 129-135
Zugang: zum Volltext
ähnliche Vorschläge
1998
zeige Details
13
Ross, Mark T., Grafham, Darren V., ... The DNA sequence of the human X chromosome
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 434, No. 7031 (2005), p. 325-337
Zugang: zum Volltext
ähnliche Vorschläge
2005