Robinow syndrome.

av Van Steensel, M
Publicerad 1998

Mirror hands and feet.

av van Steensel, M A
Publicerad 1997

Molecular Genetic Approaches to Skin Disease: Keratins and Keratinisation

av van Steensel, M A M, Steijlen, P M, Rees, J L
I publikationen J R Coll Physicians Lond (1997)

A missense mutation in the type II hair keratin hHb3 is associated with monilethrix

av van Steensel, M A M, Steijlen, P, Bladergroen, R, Vermeer, M, van Geel, M
Publicerad 2005

A novel mutation in NLRC4 in a large pedigree with an anakinra responsive autoinflammatory disease

av Volker-Touw, N, de Koning, H, van Kempen, T, Oberndorff, K, van Steensel, M, Giltay, J, Boes, M, de Kovel, C, Simon, A, Frenkel, J, van Gijn, M
I publikationen Pediatr Rheumatol Online J (2015)

Mutations in the Gene Encoding the Wnt-Signaling Component R-Spondin 4 (RSPO4) Cause Autosomal Recessive Anonychia

av Bergmann, C. , Senderek, J. , Anhuf, D. , Thiel, C. T. , Ekici, A. B. , Poblete-Gutiérrez, P. , van Steensel, M. , Seelow, D. , Nürnberg, G. , Schild, H. H. , Nürnberg, P. , Reis, A. , Frank, J. , Zerres, K. 
Publicerad 2006

Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27.

av van Bokhoven, H, Jung, M, Smits, A P, van Beersum, S, Rüschendorf, F, van Steensel, M, Veenstra, M, Tuerlings, J H, Mariman, E C, Brunner, H G, Wienker, T F, Reis, A, Ropers, H H, Hamel, B C
Publicerad 1999

The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing.

av van Steensel, M, Smith, F J, Steijlen, P M, Kluijt, I, Stevens, H P, Messenger, A, Kremer, H, Dunnill, M G, Kennedy, C, Munro, C S, Doherty, V R, McGrath, J A, Covello, S P, Coleman, C M, Uitto, J, McLean, W H
Publicerad 1999

Ehlers-Danlos Arthrochalasia type (VIIA-B) – expanding the phenotype: from prenatal life through adulthood

av Klaassens, M., Reinstein, E., Hilhorst-Hofstee, Y., Schrander, J.J.P., Malfait, F., Staal, H., ten Have, L.C., Blaauw, J., Roggeveen, H.C.J., Krakow, D., De Paepe, A., van Steensel, M.A.M., Pals, G., Graham, J. M., Schrander-Stumpel, C.T.R.M.
Publicerad 2011

Renal cancer and pneumothorax risk in Birt–Hogg–Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families

av Houweling, A C, Gijezen, L M, Jonker, M A, van Doorn, M B A, Oldenburg, R A, van Spaendonck-Zwarts, K Y, Leter, E M, van Os, T A, van Grieken, N C T, Jaspars, E H, de Jong, M M, Bongers, E M H F, Johannesma, P C, Postmus, P E, van Moorselaar, R J A, van Waesberghe, J-Htm, Starink, T M, van Steensel, M A M, Gille, J J P, Menko, F H
Publicerad 2011