Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients

Author:

Arnold Jelena S.,Braunstein Evan M.,Ohyama Takahiro,Groves Andrew K.,Adams Joe C.,Brown M. Christian,Morrow Bernice E.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference41 articles.

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2. Emanuel, B.S., McDonald-McGinn, D., Saitta, S.C. and Zackai, E.H. ( 2001 ) The 22q11.2 deletion syndrome. Adv. Pediatr. , 48 , 39 –73.

3. McDonald-McGinn, D.M., Kirschner, R., Goldmuntz, E., Sullivan, K., Eicher, P., Gerdes, M., Moss, E., Solot, C., Wang, P., Jacobs, I. et al . ( 1999 ) The Philadelphia story: the 22q11.2 deletion: report on 250 patients. Genet. Couns. , 10 , 11 –24.

4. Greenberg, F. ( 1989 ) What defines DiGeorge anomaly? J. Pediatr. , 115 , 412 –413.

5. Schuknecht, H.F. ( 1980 ) Mondini dysplasia: a clinical and pathological study. Ann. Otol. Rhinol. Laryngol. Suppl. , 89 , 1 –23.

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