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Journal of Medical Genetics|November 1, 1996
Rothmund-Thomson syndrome: two case reports show heterogeneous cutaneous abnormalities, an association with genetically programmed ageing changes, and increased chromosomal radiosensitivityB Kerr, G S Ashcroft, D Scott, et al.American Journal of Medical Genetics|April 10, 1995
Prenatal diagnosis of Smith-Lemli-Opitz syndromeJ M McGaughran, P T Clayton, K A Mills, et al.The Quarterly Journal of Medicine|August 1, 1992
A clinical study of type 2 neurofibromatosisD G Evans, S M Huson, D Donnai, et al.International Journal of Pancreatology : Official Journal of the International Association of Pancreatology|January 1, 1988
Chronic pancreatitis, HLA and autoimmunityR J Anderson, P A Dyer, D Donnai, et al.Journal of Medical Genetics|March 1, 1990
Cranial hemihypertrophy and neurodevelopmental prognosisJ C Dean, G F Cole, R E Appleton, et al.European Journal of Human Genetics : EJHG|January 1, 1994
A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28A R Curtis, S Lindsay, E Boye, et al.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.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.Pageof 13