Hodgkins P - Search Results

1

Kabuki syndrome: new ocular findings but no evidence of 8p22-p23.1 duplications in a clinically defined cohort.

Turner C, Lachlan K, Amerasinghe N, Hodgkins P, Maloney V, Barber J, Temple IK. Turner C, et al. Among authors: hodgkins p. Eur J Hum Genet. 2005 Jun;13(6):716-20. doi: 10.1038/sj.ejhg.5201377. Eur J Hum Genet. 2005. PMID: 15785777

2

Hereditary hyperferritinemia cataract syndrome: ocular, genetic, and biochemical findings.

Ismail AR, Lachlan KL, Mumford AD, Temple IK, Hodgkins PR. Ismail AR, et al. Among authors: hodgkins pr. Eur J Ophthalmol. 2006 Jan-Feb;16(1):153-60. doi: 10.1177/112067210601600125. Eur J Ophthalmol. 2006. PMID: 16496261

3

Anterior chamber eye anomalies, redundant skin and syndactyly--a new syndrome associated with breakpoints at 2q37.2 and 7q36.3.

Temple IK, Browne C, Hodgkins P. Temple IK, et al. Among authors: hodgkins p. Clin Dysmorphol. 1999 Jul;8(3):157-63. Clin Dysmorphol. 1999. PMID: 10457847

4

Fibromatosis (desmoid tumor) involving the orbit and cheek.

Amerasinghe N, Rogers S, Rowlandson P, Kohler J, Hodgkins P. Amerasinghe N, et al. Among authors: hodgkins p. J AAPOS. 2006 Oct;10(5):479-81. doi: 10.1016/j.jaapos.2006.04.008. Epub 2006 Sep 7. J AAPOS. 2006. PMID: 17070488 No abstract available.

5

Fine mapping of the X-linked recessive congenital idiopathic nystagmus locus at Xq24-q26.3.

Self JE, Ennis S, Collins A, Shawkat F, Harris CM, Mackey DA, Hodgkins PR, Temple IK, Chen X, Lotery AJ. Self JE, et al. Mol Vis. 2006 Oct 18;12:1211-6. Mol Vis. 2006. PMID: 17102799 Free article.

6

Persistent Fetal Vasculature and Severe Protein C Deficiency.

Douglas AG, Rafferty H, Hodgkins P, Nagra A, Foulds NC, Morgan M, Temple IK. Douglas AG, et al. Among authors: hodgkins p. Mol Syndromol. 2010;1(2):82-86. doi: 10.1159/000302372. Epub 2010 Apr 23. Mol Syndromol. 2010. PMID: 21045961 Free PMC article.

7

New case of "apple-peel" intestinal atresia and ocular anomalies with mosaic variegated aneuploidy.

Bower KL, Dennis NR, Wellesley D, Williams CP, Hodgkins P, Tyreman C, Browne CE, Barber JC. Bower KL, et al. Among authors: hodgkins p. Am J Med Genet A. 2003 Mar 1;117A(2):200-1. doi: 10.1002/ajmg.a.10035. Am J Med Genet A. 2003. PMID: 12567426 No abstract available.

8

Frontonasal dysplasia with optic disc anomalies and other midline craniofacial defects: a report of six cases.

Lees MM, Hodgkins P, Reardon W, Taylor D, Stanhope R, Jones B, Hayward R, Hockley AD, Baraitser M, Winter RM. Lees MM, et al. Among authors: hodgkins p. Clin Dysmorphol. 1998 Jul;7(3):157-62. doi: 10.1097/00019605-199807000-00001. Clin Dysmorphol. 1998. PMID: 9689987 Review.

9

Joubert syndrome: long-term follow-up.

Hodgkins PR, Harris CM, Shawkat FS, Thompson DA, Chong K, Timms C, Russell-Eggitt I, Taylor DS, Kriss A. Hodgkins PR, et al. Dev Med Child Neurol. 2004 Oct;46(10):694-9. doi: 10.1017/s0012162204001161. Dev Med Child Neurol. 2004. PMID: 15473174 Free article.

10

Familial congenital saccade initiation failure and isolated cerebellar vermis hypoplasia.

Harris CM, Hodgkins PR, Kriss A, Chong WK, Thompson DA, Mezey LE, Shawkat FS, Taylor DS, Wilson J. Harris CM, et al. Among authors: hodgkins pr. Dev Med Child Neurol. 1998 Nov;40(11):775-9. doi: 10.1111/j.1469-8749.1998.tb12347.x. Dev Med Child Neurol. 1998. PMID: 9881808 Free article.

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