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Tan, TY, Collins, A, James, PA, McGillivray, G, Stark, Z, Gordon, CT, Leventer, RJ, Pope, K, Forbes, R, Crolla, JA, et al.
Phenotypic variability of distal 22q11.2 copy number abnormalities..
Am J Med Genet A
155A(7)
:
1623 -1633
2011
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Stark, Z, Storen, R, Bennetts, B, Savarirayan, R, Jamieson, RV.
Isolated hypogonadotropic hypogonadism with SOX2 mutation and anophthalmia/microphthalmia in offspring..
Eur J Hum Genet
19(7)
:
753 -756
2011
view publication
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Lasocki, AL, Stark, Z, Orchard, D.
A case of mosaic Goltz syndrome (focal dermal hypoplasia) in a male patient..
Australas J Dermatol
52(1)
:
48 -51
2011
view publication
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Stark, Z, Ryan, MM, Bruno, DL, Burgess, T, Savarirayan, R.
Atypical Silver-Russell phenotype resulting from maternal uniparental disomy of chromosome 7..
Am J Med Genet A
152A(9)
:
2342 -2345
2010
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Laugel, V, Dalloz, C, Durand, M, Sauvanaud, F, Kristensen, U, Vincent, MC, Pasquier, L, Odent, S, Cormier-Daire, V, Gener, B, et al.
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome..
Hum Mutat
31(2)
:
113 -126
2010
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