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

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

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

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

Parental somatic and germ-line mosaicism for a FBN2 mutation and analysis of FBN2 transcript levels in dermal fibroblasts.

Por Putnam, E A, Park, E S, Aalfs, C M, Hennekam, R C, Milewicz, D M
Publicado em 1997

Oculocerebrocutaneous syndrome.

Por Bleeker-Wagemakers, L M, Hamel, B C, Hennekam, R C, Beemer, F A, Oorthuys, H W
Publicado em 1990

A male carrier for Duchenne muscular dystrophy.

Por Hennekam, R C, Veenema, H, Bakker, E, Jennekens, F G, Te Velde, E R, de Pater, J
Publicado em 1989

RET gene mutations are not a common cause of congenital solitary functioning kidney in adults

Por Oram, Richard A., Edghill, Emma L., Woolf, Adrian S., Hennekam, R. C., Ellard, Sian, Hattersley, A. T., Bingham, Coralie
Publicado no NDT Plus (2009)

Familial neurofibromatosis type 1 associated with an overgrowth syndrome resembling Weaver syndrome.

Por van Asperen, C J, Overweg-Plandsoen, W C, Cnossen, M H, van Tijn, D A, Hennekam, R C
Publicado em 1998

Further delineation of the partial proximal trisomy 10q syndrome.

Por Aalfs, C M, Hoovers, J M, Nieste-Otter, M A, Mannens, M M, Hennekam, R C, Leschot, N J
Publicado em 1995

Mutation screening in Börjeson‐Forssman‐Lehmann syndrome: identification of a novel de novo PHF6 mutation in a female patient

Por Crawford, J, Lower, K M, Hennekam, R C M, Van Esch, H, Mégarbané, A, Lynch, S A, Turner, G, Gécz, J
Publicado em 2006