K. Small

发表

Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease.

A. Ciccodicola, M. D'urso, S. Bione, 1995, Human molecular genetics.

Genomic organization and cloning of the human homologue of murine Sipa-1.

M. Sawicki, N. Udar, K. Small, 1998, Gene.

1 Emerin deletions occurring on both Xq28 inversion

S. Warren, K. Small, 1997 .

Identification of BPESC1, a novel gene disrupted by a balanced chromosomal translocation, t(3;4)(q23;p15.2), in a patient with BPES.

Y. Fukushima, A. Palotie, A. De Paepe, 2000, Genomics.

Resolution of spontaneous bleeding events but failure of pregnancy in fibrinogen-deficient mice.

J. Degen, N. Jensen, K. Small, 1995, Genes & development.

Hoxa 11 structure, extensive antisense transcription, and function in male and female fertility.

D. Witte, S. Potter, H. Hsieh-Li, 1995, Development.

Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeats

S. Warren, J. Iber, K. Small, 1997, Nature Genetics.

Emerin deletions occurring on both Xq28 inversion backgrounds.

S. Warren, K. Small, Stephen T. Warren, 1998, Human molecular genetics.

Homeotic transformations and limb defects in Hox A11 mutant mice.

S. Potter, K. Small, S. Potter, 1993, Genes & development.

Altered forebrain and hindbrain development in mice mutant for the Gsh-2 homeobox gene.

S. Potter, S. Pixley, J. C. Szucsik, 1997, Developmental biology.

Isolation and characterization of the complete mouse emerin gene

S. Warren, K. Small, M. Wagener, 1997, Mammalian Genome.

Purified Recombinant Fmrp Exhibits Selective RNA Binding as an Intrinsic Property of the Fragile X Mental Retardation Protein*

C. Gunter, S. Warren, V. Brown, 1998, The Journal of Biological Chemistry.

Gsh‐1, an orphan Hox gene, is required for normal pituitary development.

S. Potter, M. Valerius, K. Small, 1996, The EMBO journal.

Analysis of FMRP, the protein deficient in fragile X syndrome

S. Warren, K. Small, 1995 .