Suthers GK - Search Results

1

Mutation detection in FGFR2 craniosynostosis syndromes.

Hollway GE, Suthers GK, Haan EA, Thompson E, David DJ, Gecz J, Mulley JC. Hollway GE, et al. Among authors: suthers gk. Hum Genet. 1997 Feb;99(2):251-5. doi: 10.1007/s004390050348. Hum Genet. 1997. PMID: 9048930

2

Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome.

Suthers GK, Mulley JC, Voelckel MA, Dahl N, Väisänen ML, Steinbach P, Glass IA, Schwartz CE, van Oost BA, Thibodeau SN, et al. Suthers GK, et al. Am J Hum Genet. 1991 Mar;48(3):460-7. Am J Hum Genet. 1991. PMID: 1671806 Free PMC article.

3

Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree.

Suthers GK, Manson JI, Stern LM, Haan EA, Mulley JC. Suthers GK, et al. J Med Genet. 1989 Apr;26(4):251-4. doi: 10.1136/jmg.26.4.251. J Med Genet. 1989. PMID: 2716035 Free PMC article.

4

Fragile X syndrome and nephrogenic diabetes insipidus.

Suthers GK, Turner G, Mulley JC. Suthers GK, et al. Am J Med Genet. 1988 May-Jun;30(1-2):231-6. doi: 10.1002/ajmg.1320300123. Am J Med Genet. 1988. PMID: 3177449

5

A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14.

Suthers GK, Turner G, Mulley JC. Suthers GK, et al. Am J Med Genet. 1988 May-Jun;30(1-2):485-91. doi: 10.1002/ajmg.1320300151. Am J Med Genet. 1988. PMID: 3177466

6

New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.

Cox TC, Allen LR, Cox LL, Hopwood B, Goodwin B, Haan E, Suthers GK. Cox TC, et al. Among authors: suthers gk. Hum Mol Genet. 2000 Oct 12;9(17):2553-62. doi: 10.1093/hmg/9.17.2553. Hum Mol Genet. 2000. PMID: 11030761

7

A BclI RFLP for DXS296 (VK21) near the fragile X.

Yu S, Suthers GK, Mulley JC. Yu S, et al. Among authors: suthers gk. Nucleic Acids Res. 1990 Feb 11;18(3):690. doi: 10.1093/nar/18.3.690-a. Nucleic Acids Res. 1990. PMID: 1968627 Free PMC article. No abstract available.

8

Deafness due to Pro250Arg mutation of FGFR3.

Hollway GE, Suthers GK, Battese KM, Turner AM, David DJ, Mulley JC. Hollway GE, et al. Among authors: suthers gk. Lancet. 1998 Mar 21;351(9106):877-8. doi: 10.1016/S0140-6736(98)24012-8. Lancet. 1998. PMID: 9525367 No abstract available.

9

Fronto-facio-nasal dysplasia.

Suthers G, David D, Clark B. Suthers G, et al. Clin Dysmorphol. 1997 Jul;6(3):245-9. doi: 10.1097/00019605-199707000-00008. Clin Dysmorphol. 1997. PMID: 9220195 Review.

10

Linkage homogeneity near the fragile X locus in normal and fragile X families.

Suthers GK, Mulley JC, Voelckel MA, Dahl N, Väisänen ML, Steinbach P, Glass IA, Schwartz CE, van Oost BA, Thibodeau SN, et al. Suthers GK, et al. Genomics. 1991 Jul;10(3):576-82. doi: 10.1016/0888-7543(91)90438-k. Genomics. 1991. PMID: 1889808

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