Baynam G - Search Results

1

Monitoring of Therapy for Mucopolysaccharidosis Type I Using Dysmorphometric Facial Phenotypic Signatures.

Kung S, Walters M, Claes P, LeSouef P, Goldblatt J, Martin A, Balasubramaniam S, Baynam G. Kung S, et al. Among authors: baynam g. JIMD Rep. 2015;22:99-106. doi: 10.1007/8904_2015_417. Epub 2015 Mar 3. JIMD Rep. 2015. PMID: 25732999 Free PMC article.

2

A case of 3q29 microdeletion with novel features and a review of cytogenetically visible terminal 3q deletions.

Baynam G, Goldblatt J, Townshend S. Baynam G, et al. Clin Dysmorphol. 2006 Jul;15(3):145-148. doi: 10.1097/01.mcd.0000198934.55071.ee. Clin Dysmorphol. 2006. PMID: 16760732 Review.

3

Associations of a novel IL4RA polymorphism, Ala57Thr, in Greenlander Inuit.

Khoo SK, Zhang G, Backer V, Porsbjerg C, Nepper-Christensen S, Creegan R, Baynam G, de Klerk N, Rossi GA, Hagel I, Di Prisco MC, Lynch N, Britton J, Hall I, Musk AW, Goldblatt J, Le Souëf PN; Greenlandic Population Study Group. Khoo SK, et al. Among authors: baynam g. J Allergy Clin Immunol. 2006 Sep;118(3):627-34. doi: 10.1016/j.jaci.2006.05.009. Epub 2006 Jun 27. J Allergy Clin Immunol. 2006. PMID: 16950281

4

Parental smoking impairs vaccine responses in children with atopic genotypes.

Baynam G, Khoo SK, Rowe J, Zhang G, Laing I, Hayden C, Kusel M, DeKlerk N, Sly P, Goldblatt J, Holt P, LeSouef P. Baynam G, et al. J Allergy Clin Immunol. 2007 Feb;119(2):366-74. doi: 10.1016/j.jaci.2006.09.018. Epub 2006 Oct 23. J Allergy Clin Immunol. 2007. PMID: 17291854

5

Deletion of 8p23.1 with features of Cornelia de Lange syndrome and congenital diaphragmatic hernia and a review of deletions of 8p23.1 to 8pter? A further locus for Cornelia de Lange syndrome.

Baynam G, Goldblatt J, Walpole I. Baynam G, et al. Am J Med Genet A. 2008 Jun 15;146A(12):1565-70. doi: 10.1002/ajmg.a.32095. Am J Med Genet A. 2008. PMID: 18470924 Review.

6

Gender-specific effects of cytokine gene polymorphisms on childhood vaccine responses.

Baynam G, Zhang G, Khoo SK, Sly P, Holt P, Goldblatt J, Le Souëf PN. Baynam G, et al. Vaccine. 2008 Jul 4;26(29-30):3574-9. doi: 10.1016/j.vaccine.2008.05.011. Epub 2008 May 27. Vaccine. 2008. PMID: 18547691

7

A c.1019A > G mutation in FGFR2, which predicts p.Tyr340Cys, in a lethally malformed fetus with Pfeiffer syndrome and multiple pterygia.

Baynam G, Smith N, Goldblatt J. Baynam G, et al. Am J Med Genet A. 2008 Sep 1;146A(17):2301-3. doi: 10.1002/ajmg.a.32443. Am J Med Genet A. 2008. PMID: 18671283 No abstract available.

8

Craniometaphyseal dysplasia and chondrocalcinosis cosegregating in a family with an ANKH mutation.

Baynam G, Goldblatt J, Schofield L. Baynam G, et al. Am J Med Genet A. 2009 Jun;149A(6):1331-3. doi: 10.1002/ajmg.a.32875. Am J Med Genet A. 2009. PMID: 19449425 No abstract available.

9

The importance of environment on respiratory genotype/phenotype relationships in the Inuit.

Candelaria PV, Backer V, Khoo SK, Bizzintino JA, Hayden CM, Baynam G, Laing IA, Zhang G, Porsbjerg C, Goldblatt J, Le Souëf PN; Greenlandic Study Population Group. Candelaria PV, et al. Among authors: baynam g. Allergy. 2010 Feb;65(2):229-37. doi: 10.1111/j.1398-9995.2009.02145.x. Epub 2009 Oct 1. Allergy. 2010. PMID: 19796192

10

A recurrence of a hydrop lethal skeletal dysplasia showing similarity to Desbuquois dysplasia and a proposed new sign: the Upsilon sign.

Baynam G, Kiraly-Borri C, Goldblatt J, Dickinson JE, Jevon GP, Overkov A. Baynam G, et al. Am J Med Genet A. 2010 Apr;152A(4):966-9. doi: 10.1002/ajmg.a.33264. Am J Med Genet A. 2010. PMID: 20358610

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