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Journal of Medical Genetics|February 1, 1986
The lethal multiple congenital anomaly syndrome of polydactyly, sex reversal, renal hypoplasia, and unilobular lungsD Donnai, I D Young, W G Owen, et al.American Journal of Medical Genetics|February 11, 1997
Diaphragmatic hernia-exomphalos-hypertelorism syndrome: a new case and further evidence of autosomal recessive inheritanceK W Gripp, D Donnai, C L Clericuzio, et al.Nature Genetics|August 1, 1994
A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1A E Hughes, V E Newton, X Z Liu, et al.Cancer Research|December 15, 1994
Deletion mapping on the short arm of chromosome 3 in squamous cell carcinoma of the oral cavityC L Wu, P Sloan, A P Read, et al.Neuromuscular Disorders : NMD|January 1, 1991
X-linked and FSH dystrophies in one familyB R Lecky, J M MacKenzie, A P Read, et al.Clinical and Experimental Immunology|February 1, 1988
The expression of CD18 is increased on Trisomy 21 (Down syndrome) lymphoblastoid cellsG M Taylor, A Williams, S W D'Souza, et al.Journal of Medical Genetics|December 10, 2002
Comparison of genetic services with and without genetic registers: access and attitudes to genetic counselling services among relatives of genetic clinic patientsL Kerzin-Storrar, C Wright, P R Williamson, et al.Journal of Medical Genetics|December 1, 1992
A genetic study of type 2 neurofibromatosis in the United Kingdom. II. Guidelines for genetic counsellingD G Evans, S M Huson, D Donnai, et al.Clinical Genetics|February 17, 2015
Dysmorphology services: a snapshot of current practices and a vision for the futureS Douzgou, E Chervinsky, Y Gyftodimou, et al.Journal of Medical Genetics|July 25, 1998
Smith-Lemli-Opitz syndrome: a variable clinical and biochemical phenotypeA K Ryan, K Bartlett, P Clayton, et al.Pageof 19