Another human homologue for the mouse mutant disorganisation.

Por Hennekam, R C
Publicado em 1992

Hereditary multiple exostoses.

Por Hennekam, R C
Publicado em 1991

Spastic paraplegia, dysarthria, brachydactyly, and cone shaped epiphyses: confirmation of the Fitzsimmons syndrome.

Por Hennekam, R C
Publicado em 1994

The Smith-Lemli-Opitz syndrome

Por Kelley, R., Hennekam, R.
Publicado em 2000

Further delineation of the Yunis-Varon syndrome.

Por Hennekam, R C, Vermeulen-Meiners, C
Publicado em 1989

Ectrodactyly in sisters and half sisters.

Por Hennekam, R C, Lommen, E J
Publicado em 1988

Marfan syndrome.

Por De Paepe, A, Hennekam, R C
Publicado em 1997

Acute lymphoblastic leukaemia in a patient with cardiofaciocutaneous syndrome

Por VAN DEN BERG, H., HENNEKAM, R.
Publicado em 1999

3-M syndrome and intracerebral aneurysms.

Por Hennekam, R C, Limburg, M, Pals, G
Publicado em 1994

Acquired alopecia, mental retardation, short stature, microcephaly, and optic atrophy.

Por Hennekam, R C, Renckens-Wennen, E G
Publicado em 1990

Dermal eccrine cylindromatosis.

Por van Balkom, I D, Hennekam, R C
Publicado em 1994

De Lange syndrome: subjective and objective comparison of the classical and mild phenotypes.

Por Allanson, J E, Hennekam, R C, Ireland, M
Publicado em 1997

A Microdeletion at 12q24.31 Can Mimic Beckwith-Wiedemann Syndrome Neonatally

Por Baple, E., Palmer, R., Hennekam, R.C.M.
Publicado em 2010

Ocular features in Rubinstein-Taybi syndrome: investigation of 24 patients and review of the literature

Por van Genderen, M. M, Kinds, G., Riemslag, F., Hennekam, R.
Publicado em 2000

Incidence and molecular mechanism of aberrant splicing owing to a G→C splice acceptor site mutation causing Smith-Lemli-Opitz syndrome

Por WATERHAM, H, OOSTHEIM, W, ROMEIJN, G, WANDERS, R, HENNEKAM, R
Publicado em 2000

A Duty To Warn Relatives in Clinical Genetics: Arguably ‘Fair just and reasonable’ in English Law?

Por Mitchell, C, Ploem, M C, Hennekam, R C M, Kaye, J
Publicado no Tottels J Prof Neglig (2016)

Syndromic ectrodactyly with severe limb, ectodermal, urogenital, and palatal defects maps to chromosome 19.

Por O'Quinn, J R, Hennekam, R C, Jorde, L B, Bamshad, M
Publicado em 1998

Congenital abnormalities reported in Pelger-Huët homozygosity as compared to Greenberg/HEM dysplasia: highly variable expression of allelic phenotypes

Por Oosterwijk, J, Mansour, S, van Noort, G, Waterham, H, Hall, C, Hennekam, R
Publicado em 2003

Natural history of cardiovascular manifestations in Marfan syndrome

Por van Karnebeek, C D M, Naeff, M, Mulder, B, Hennekam, R, Offringa, M
Publicado em 2001

Novel mutations in the gene SALL4 provide further evidence for acro-renal-ocular and Okihiro syndromes being allelic entities, and extend the phenotypic spectrum

Por Borozdin, W, Wright, M, Hennekam, R, Hannibal, M, Crow, Y, Neumann, T, Kohlhase, J
Publicado em 2004