Another human homologue for the mouse mutant disorganisation.

gan Hennekam, R C
Cyhoeddwyd 1992

Hereditary multiple exostoses.

gan Hennekam, R C
Cyhoeddwyd 1991

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

gan Hennekam, R C
Cyhoeddwyd 1994

Further delineation of the Yunis-Varon syndrome.

gan Hennekam, R C, Vermeulen-Meiners, C
Cyhoeddwyd 1989

Ectrodactyly in sisters and half sisters.

gan Hennekam, R C, Lommen, E J
Cyhoeddwyd 1988

Marfan syndrome.

gan De Paepe, A, Hennekam, R C
Cyhoeddwyd 1997

3-M syndrome and intracerebral aneurysms.

gan Hennekam, R C, Limburg, M, Pals, G
Cyhoeddwyd 1994

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

gan Hennekam, R C, Renckens-Wennen, E G
Cyhoeddwyd 1990

Dermal eccrine cylindromatosis.

gan van Balkom, I D, Hennekam, R C
Cyhoeddwyd 1994

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

gan Allanson, J E, Hennekam, R C, Ireland, M
Cyhoeddwyd 1997

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

gan Baple, E., Palmer, R., Hennekam, R.C.M.
Cyhoeddwyd 2010

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

gan Mitchell, C, Ploem, M C, Hennekam, R C M, Kaye, J
Cyhoeddwyd yn Tottels J Prof Neglig (2016)

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

gan O'Quinn, J R, Hennekam, R C, Jorde, L B, Bamshad, M
Cyhoeddwyd 1998

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

gan Putnam, E A, Park, E S, Aalfs, C M, Hennekam, R C, Milewicz, D M
Cyhoeddwyd 1997

Oculocerebrocutaneous syndrome.

gan Bleeker-Wagemakers, L M, Hamel, B C, Hennekam, R C, Beemer, F A, Oorthuys, H W
Cyhoeddwyd 1990

A male carrier for Duchenne muscular dystrophy.

gan Hennekam, R C, Veenema, H, Bakker, E, Jennekens, F G, Te Velde, E R, de Pater, J
Cyhoeddwyd 1989

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

gan Oram, Richard A., Edghill, Emma L., Woolf, Adrian S., Hennekam, R. C., Ellard, Sian, Hattersley, A. T., Bingham, Coralie
Cyhoeddwyd yn NDT Plus (2009)

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

gan van Asperen, C J, Overweg-Plandsoen, W C, Cnossen, M H, van Tijn, D A, Hennekam, R C
Cyhoeddwyd 1998

Further delineation of the partial proximal trisomy 10q syndrome.

gan Aalfs, C M, Hoovers, J M, Nieste-Otter, M A, Mannens, M M, Hennekam, R C, Leschot, N J
Cyhoeddwyd 1995

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

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