Anmelden/Registrieren
Erscheinungsjahr:
 
Zurück zur geteilten Ansicht
Elaine H. Zackai

Veröffentlichungen von Elaine H. Zackai zu Zackai, Elaine H. ->
weitere Veröffentlichungen von Elaine H. Zackai:
Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene? (1995)
Human malformations similar to those in the mouse mutation disorganization (Ds) (1993)
Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes (1996)
Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic male (1988)
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly (1999)
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination (2000)
Ablepharon macrostomia syndrome with associated cutis laxa: Possible localization to 18q (1996)
Ablepharon macrostomia syndrome with associated cutis laxa: possible localization to 18q (1996)
Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patient (1999)
Discovery of a previously unrecognized microdeletion syndrome of 16p11.2–p12.2 (2007)
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes (2002)
Veröffentlichungen zu Zackai, Elaine H.
Zurück zur geteilten Ansicht
Verfasser Titel Jahr absteigend sortierenaufsteigend sortieren
zeige Details
1
Pellegrino, Joan E., Schnur, Rhonda E., ... Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene?
in: Human genetics , ISSN 1432-1203, Vol. 96 (4. 1995), p. 485-489
Zugang: zum Volltext
ähnliche Vorschläge
1995
zeige Details
2
Robin, Nathaniel H., Adewale, Olusina O., ... Human malformations similar to those in the mouse mutation disorganization (Ds)
in: Human genetics , ISSN 1432-1203, Vol. 92 (5. 1993), p. 461-464
Zugang: zum Volltext
ähnliche Vorschläge
1993
zeige Details
3
Bellus, Gary A., Gaudenz, Karin, ... Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 14, No. 2 (1996), p. 174-176
Zugang: zum Volltext
ähnliche Vorschläge
1996
zeige Details
4
Münke, Maximilian, Page, David C., ... Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic male
in: Human genetics , ISSN 1432-1203, Vol. 80 (3. 1988), p. 219-223
Zugang: zum Volltext
ähnliche Vorschläge
1988
zeige Details
5
Wallis, Deeann E., Roessler, Erich, ... Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 22, No. 2 (1999), p. 196-198
Zugang: zum Volltext
ähnliche Vorschläge
1999
zeige Details
6
Gripp, Karen W., Wotton, David, ... Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 25, No. 2 (2000), p. 205-208
Zugang: zum Volltext
ähnliche Vorschläge
2000
zeige Details
7
Pellegrino, Joan E., Schnur, Rhonda E., ... Ablepharon macrostomia syndrome with associated cutis laxa: Possible localization to 18q
in: Human genetics , ISSN 1432-1203, Vol. 97 (4. 1996), p. 532-536
Zugang: zum Volltext
ähnliche Vorschläge
1996
zeige Details
8
Pellegrino, Joan E., Schnur, Rhonda E., ... Ablepharon macrostomia syndrome with associated cutis laxa: possible localization to 18q
in: Human genetics , ISSN 1432-1203, Vol. 97 (4. 1996), p. 532-536
Zugang: zum Volltext
ähnliche Vorschläge
1996
zeige Details
9
Gecz, J., Baker, Elizabeth, ... Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication...
in: Human genetics , ISSN 1432-1203, Vol. 104 (1. 1999), p. 56-63
Zugang: zum Volltext
ähnliche Vorschläge
1999
zeige Details
10
Ballif, Blake C, Hornor, Sara A, ... Discovery of a previously unrecognized microdeletion syndrome of 16p11.2–p12.2
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 9 (2007), p. 1071-1073
Zugang: zum Volltext
ähnliche Vorschläge
2007
zeige Details
11
Kondo, Shinji, Schutte, Brian C., ... Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 32, No. 2 (2002), p. 285-289
Zugang: zum Volltext
ähnliche Vorschläge
2002