Robin NH - Search Results

1

The use of genetic testing in the evaluation of hearing impairment in a child.

Robin NH, Prucka SK, Woolley AL, Smith RJ. Robin NH, et al. Curr Opin Pediatr. 2005 Dec;17(6):709-12. doi: 10.1097/01.mop.0000181469.56484.5f. Curr Opin Pediatr. 2005. PMID: 16282775 Review.

2

Parental attitudes toward genetic testing for pediatric deafness.

Brunger JW, Murray GS, O'Riordan M, Matthews AL, Smith RJ, Robin NH. Brunger JW, et al. Among authors: robin nh. Am J Hum Genet. 2000 Dec;67(6):1621-5. doi: 10.1086/316901. Epub 2000 Nov 2. Am J Hum Genet. 2000. PMID: 11062052 Free PMC article.

3

Pediatric otolaryngologists' knowledge and understanding of genetic testing for deafness.

Robin NH, Dietz C, Arnold JE, Smith RJ. Robin NH, et al. Arch Otolaryngol Head Neck Surg. 2001 Aug;127(8):937-40. doi: 10.1001/archotol.127.8.937. Arch Otolaryngol Head Neck Surg. 2001. PMID: 11493201

4

Genetic testing for deafness--GJB2 and SLC26A4 as causes of deafness.

Smith RJ, Robin NH. Smith RJ, et al. Among authors: robin nh. J Commun Disord. 2002 Jul-Aug;35(4):367-77. doi: 10.1016/s0021-9924(02)00091-6. J Commun Disord. 2002. PMID: 12160355

5

Clefting, amniotic bands, and polydactyly: a distinct phenotype that supports an intrinsic mechanism for amniotic band sequence.

Robin NH, Franklin J, Prucka S, Ryan AB, Grant JH. Robin NH, et al. Am J Med Genet A. 2005 Sep 1;137A(3):298-301. doi: 10.1002/ajmg.a.30885. Am J Med Genet A. 2005. PMID: 16088913 Review.

6

The multidisciplinary evaluation and management of cleft lip and palate.

Robin NH, Baty H, Franklin J, Guyton FC, Mann J, Woolley AL, Waite PD, Grant J. Robin NH, et al. South Med J. 2006 Oct;99(10):1111-20. doi: 10.1097/01.smj.0000209093.78617.3a. South Med J. 2006. PMID: 17100032 Review.

7

Pediatric otolaryngologists' use of genetic testing.

Duncan RD, Prucka S, Wiatrak BJ, Smith RJ, Robin NH. Duncan RD, et al. Among authors: robin nh. Arch Otolaryngol Head Neck Surg. 2007 Mar;133(3):231-6. doi: 10.1001/archotol.133.3.231. Arch Otolaryngol Head Neck Surg. 2007. PMID: 17372079

8

Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter).

Mikhail FM, Sathienkijkanchai A, Robin NH, Prucka S, Biggerstaff JS, Komorowski J, Andersson R, Bruder CE, Piotrowski A, Diaz de Ståhl T, Dumanski JP, Carroll AJ. Mikhail FM, et al. Among authors: robin nh. Am J Med Genet A. 2007 Aug 1;143A(15):1760-6. doi: 10.1002/ajmg.a.31821. Am J Med Genet A. 2007. PMID: 17603794

9

Isolated facial hemihyperplasia: manifestation of Beckwith-Wiedemann syndrome.

Sathienkijkanchai A, Prucka SK, Grant JH, Robin NH. Sathienkijkanchai A, et al. Among authors: robin nh. J Craniofac Surg. 2008 Jan;19(1):279-83. doi: 10.1097/SCS.0b013e31815ca067. J Craniofac Surg. 2008. PMID: 18216702

10

The use of role-play to enhance medical student understanding of genetic counseling.

McIlvried DE, Prucka SK, Herbst M, Barger C, Robin NH. McIlvried DE, et al. Among authors: robin nh. Genet Med. 2008 Oct;10(10):739-44. doi: 10.1097/GIM.0b013e318187762e. Genet Med. 2008. PMID: 18813131 Free article.

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