Bankier A - Search Results

1

SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literature.

Nanni L, Ming JE, Du Y, Hall RK, Aldred M, Bankier A, Muenke M. Nanni L, et al. Among authors: bankier a. Am J Med Genet. 2001 Jul 22;102(1):1-10. doi: 10.1002/1096-8628(20010722)102:1<1::aid-ajmg1336>3.0.co;2-u. Am J Med Genet. 2001. PMID: 11471164 Review.

2

CHARGE association: clinical manifestations and developmental outcome.

Harvey AS, Leaper PM, Bankier A. Harvey AS, et al. Among authors: bankier a. Am J Med Genet. 1991 Apr 1;39(1):48-55. doi: 10.1002/ajmg.1320390112. Am J Med Genet. 1991. PMID: 1867265

3

Geleophysic dysplasia.

Wraith JE, Bankier A, Chow CW, Danks DM, Sardharwalla IB. Wraith JE, et al. Among authors: bankier a. Am J Med Genet. 1990 Feb;35(2):153-6. doi: 10.1002/ajmg.1320350202. Am J Med Genet. 1990. PMID: 2090119

4

Gingival fibromatosis and Klippel-Trénaunay-Weber syndrome. Case report.

Hallett KB, Bankier A, Chow CW, Bateman J, Hall RK. Hallett KB, et al. Among authors: bankier a. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1995 May;79(5):578-82. doi: 10.1016/s1079-2104(05)80099-x. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1995. PMID: 7600221

5

Asymmetry and skin pigmentary anomalies in chromosome mosaicism.

Woods CG, Bankier A, Curry J, Sheffield LJ, Slaney SF, Smith K, Voullaire L, Wellesley D. Woods CG, et al. Among authors: bankier a. J Med Genet. 1994 Sep;31(9):694-701. doi: 10.1136/jmg.31.9.694. J Med Genet. 1994. PMID: 7815438 Free PMC article.

6

Solitary median maxillary central incisor, short stature, choanal atresia/midnasal stenosis (SMMCI) syndrome.

Hall RK, Bankier A, Aldred MJ, Kan K, Lucas JO, Perks AG. Hall RK, et al. Among authors: bankier a. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1997 Dec;84(6):651-62. doi: 10.1016/s1079-2104(97)90368-1. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1997. PMID: 9431535 Review.

7

Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Cantú syndrome.

Robertson SP, Kirk E, Bernier F, Brereton J, Turner A, Bankier A. Robertson SP, et al. Among authors: bankier a. Am J Med Genet. 1999 Aug 6;85(4):395-402. Am J Med Genet. 1999. PMID: 10398267

8

New case of Cole-Carpenter syndrome.

Amor DJ, Savarirayan R, Schneider AS, Bankier A. Amor DJ, et al. Among authors: bankier a. Am J Med Genet. 2000 Jun 5;92(4):273-7. doi: 10.1002/(sici)1096-8628(20000605)92:4<273::aid-ajmg10>3.0.co;2-t. Am J Med Genet. 2000. PMID: 10842295 Review.

9

Molecular analysis for genetic counselling in amelogenesis imperfecta.

Aldred MJ, Hall RK, Kilpatrick N, Bankier A, Savarirayan R, Lamandé SR, Lench NJ, Crawford PJ. Aldred MJ, et al. Among authors: bankier a. Oral Dis. 2002 Sep;8(5):249-53. doi: 10.1034/j.1601-0825.2002.02835.x. Oral Dis. 2002. PMID: 12363109

10

Focal segmental glomerulosclerosis in patients with mandibuloacral dysplasia owing to ZMPSTE24 deficiency.

Agarwal AK, Zhou XJ, Hall RK, Nicholls K, Bankier A, Van Esch H, Fryns JP, Garg A. Agarwal AK, et al. Among authors: bankier a. J Investig Med. 2006 May;54(4):208-13. doi: 10.2310/6650.2006.05068. J Investig Med. 2006. PMID: 17152860

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