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Results:
1-9
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Results: 9
Authors:
Kennerson, ML
Zhu, D
Gardner, RJM
Storey, E
Merory, J
Robertson, SP
Nicholson, GA
Citation: Ml. Kennerson et al., Dominant intermediate Charcot-Marie-Tooth neuropathy maps to chromosome 19p12-p13.2, AM J HU GEN, 69(4), 2001, pp. 883-888
Authors:
Robertson, SP
Walsh, S
Oldridge, M
Gunn, T
Becroft, D
Wilkie, AOM
Citation: Sp. Robertson et al., Linkage of otopalatodigital syndrome type 2 (OPD2) to distal Xq28: Evidence for allelism with OPD1, AM J HU GEN, 69(1), 2001, pp. 223-227
Authors:
Robertson, SP
Gattas, M
Rogers, M
Ades, LC
Citation: Sp. Robertson et al., Macrocephaly - cutis marmorata telangiectatica congenita: report of five patients and a review of the literature, CLIN DYSMOR, 9(1), 2000, pp. 1-9
Authors:
Robertson, SP
Shears, DJ
Oei, P
Winter, RM
Scambler, PJ
Aftimos, S
Savarirayan, R
Citation: Sp. Robertson et al., Homozygous deletion of SHOX in a mentally retarded male with Langer mesomelic dysplasia, J MED GENET, 37(12), 2000, pp. 959-964
Authors:
Robertson, SP
Rodda, C
Bankier, A
Citation: Sp. Robertson et al., Hypogonadotrophic hypogonadism in Roifman syndrome, CLIN GENET, 57(6), 2000, pp. 435-438
Authors:
Robertson, SP
Kirk, E
Bernier, F
Brereton, J
Turner, A
Bankier, A
Citation: Sp. Robertson et al., Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Cantu syndrome, AM J MED G, 85(4), 1999, pp. 395-402
Authors:
Robertson, SP
Bankier, A
Citation: Sp. Robertson et A. Bankier, Oromandibular limb hypogenesis complex (Hanhart syndrome): A severe adult phenotype, AM J MED G, 83(5), 1999, pp. 427-429
Authors:
Robertson, SP
Dickens, R
Savarirayan, R
Rogers, JG
Citation: Sp. Robertson et al., An autosomal dominant or X-linked osteodysplastic disorder with severe cervical involvement, AM J MED G, 83(1), 1999, pp. 17-22
Authors:
Robertson, SP
Bankier, A
Citation: Sp. Robertson et A. Bankier, Sotos syndrome and cutis laxa, J MED GENET, 36(1), 1999, pp. 51-56
Risultati:
1-9
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