Opitz G/BBB Syndrome in Xp22: Mutations in the MID1 Gene Cluster in the Carboxy-Terminal Domain-Reference-Cited by-同舟云学术

Opitz G/BBB Syndrome in Xp22: Mutations in the MID1 Gene Cluster in the Carboxy-Terminal Domain

Published:1998-09 Issue:3 Volume:63 Page:703-710
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Gaudenz Karin,Roessler Erich,Quaderi Nandita,Franco Brunella,Feldman George,Gasser David L.,Wittwer Bärbel,Montini Eugenio,Opitz John M.,Ballabio Andrea,Muenke Maximilian

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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4. Characterization of a novel cysteine/histidine-rich metal binding domain from Xenopus nuclear factor XNF7;Borden;FEBS Lett,1993

5. Opitz (BBB/G) syndrome: oral manifestations;Brooks;Am J Med Genet,1992

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