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Journal of Medical Genetics|March 1, 1994
Crouzon syndrome is not linked to craniosynostosis loci at 7p and 5qterW Reardon, L van Herwerden, C Rose, et al.Journal of Medical Genetics|September 1, 1992
The acrocallosal syndrome and Greig syndrome are not allelic disordersL A Brueton, K A Chotai, L van Herwerden, et al.Archives of Disease in Childhood|July 1, 1988
Pulmonary agenesis as part of the VACTERL sequenceS Knowles, R M Thomas, R H Lindenbaum, et al.Clinical Dysmorphology|October 1, 1996
Extreme intrauterine growth retardation, hydrocephalus and aged facial appearance: a previously unrecognized autosomal recessive disorder?R M Winter, D Shortland, A L Collins, et al.Journal of Medical Genetics|September 1, 1993
Exclusion of candidate genes from a role in cleft lip with or without cleft palate: linkage and association studiesG M Vintiner, K K Lo, S E Holder, et al.Clinical Dysmorphology|April 1, 1997
A syndrome of brachyphalangy, polydactyly and absent tibiaeM Baraitser, F Stewart, R M Winter, et al.Clinical Dysmorphology|April 1, 1996
An unusual presentation of Smith-Magenis syndrome with iris dysgenesisA J Barnicoat, H U Moller, R W Palmer, et al.Nature Genetics|September 1, 1994
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndromeW Reardon, R M Winter, P Rutland, et al.Clinical Dysmorphology|April 1, 1994
A case with blepharophimosis resembling Ohdo syndromeJ A Maat-Kievit, P J Milla, J E Collins, et al.Human Genetics|July 1, 1989
MASA syndrome: further clinical delineation and chromosomal localisationR M Winter, K E Davies, M V Bell, et al.Pageof 19