Ingrid Stec

WHSC1, a 90 kb SET Domain-Containing Gene, Expressed in Early Development and Homologous to a Drosophila Dysmorphy Gene Maps in the Wolf-Hirschhorn Syndrome Critical Region and is Fused to IgH in t(1;14) Multiple Myeloma

Ingrid Stec, Tracy J. Wright, G.J.B. van Ommen et al. · Human Molecular Genetics · 1998 · 315 citations

WHSC1L1, on Human Chromosome 8p11.2, Closely Resembles WHSC1 and Maps to a Duplicated Region Shared with 4p16.3

Ingrid Stec, Gert-Jan B. van Ommen, Johan T. den Dunnen · Genomics · 2001 · 81 citations

Chromatin, Human Chromosome 8P11.2, Closely Resembles Whsc1 +11

Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3.

Sarina G. Kant, Arie van Haeringen, E Bakker et al. · Journal of Medical Genetics · 1997 · 41 citations · Full text

Chromatin, Wolf-hirschhorn Syndrome, Mendelian Disorder +15

Estimate of severe autosomal recessive limb-girdle muscular dystrophy (LGMD2C, LGMD2D) among sporadic muscular dystrophy males: a study of 415 familes.

Ingrid Stec, B. Müller, C. R. Müller et al. · Journal of Medical Genetics · 1995 · 14 citations · Full text

Rare Diseases, Mendelian Disorder, Genetic Disorder +13

Nephropathic cystinosis (CTNS-LSB): construction of a YAC contig comprising the refined critical region on chromosome 17p13.

Ulrike Peters, Gabriele Senger, Michael Rählmann et al. · PubMed · 1997 · 12 citations · Full text