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I A Glass

Showing results (1-10 of 42) with videos related to

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Journal of Medical Genetics|June 1, 1991
X linked mental retardationI A Glass
Clinical Dysmorphology|July 1, 1994
A distinct autosomal dominant craniosynostosis-brachydactyly syndromeI A Glass, S Chapman, A D Hockley
Scottish Medical Journal|June 1, 1988
Aldosterone deficiency in infancyI A Glass, A M Wallace, T J Beattie
Clinical Dysmorphology|April 1, 1994
Ear anomalies, clefting and limb reduction defects: a new autosomal recessive condition?I A Glass, J Walford-Moore, S Chapman, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|February 7, 2001
Low maternal serum oestriol at mid-trimester may indicate a fetal disorder of cholesterol biosynthesisJ E Craig, V Savage, D Cowley, et al.
American Journal of Medical Genetics|July 12, 1996
Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardationA K Gedeon, I A Glass, J M Connor, et al.
American Journal of Medical Genetics|April 1, 1992
XLMR genes: update 1992G Neri, P Chiurazzi, F Arena, et al.
Clinical Genetics|June 14, 2000
Mild phenotype in two siblings with distal monosomy 12p13.31-->pterI A Glass, A Trenholme, L Mildenhall, et al.
Journal of Medical Genetics|February 1, 1989
Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenaseI A Glass, C A Swindlehurst, D A Aitken, et al.
Seminars in Liver Disease|March 28, 1998
Molecular genetics of congenital erythropoietic porphyriaR J Desnick, I A Glass, W Xu, et al.
Pageof 5

Showing results (1-10 of 42) with videos related to

Sort By:
Pageof 5
Journal of Medical Genetics|June 1, 1991
X linked mental retardationI A Glass
Clinical Dysmorphology|July 1, 1994
A distinct autosomal dominant craniosynostosis-brachydactyly syndromeI A Glass, S Chapman, A D Hockley
Scottish Medical Journal|June 1, 1988
Aldosterone deficiency in infancyI A Glass, A M Wallace, T J Beattie
Clinical Dysmorphology|April 1, 1994
Ear anomalies, clefting and limb reduction defects: a new autosomal recessive condition?I A Glass, J Walford-Moore, S Chapman, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|February 7, 2001
Low maternal serum oestriol at mid-trimester may indicate a fetal disorder of cholesterol biosynthesisJ E Craig, V Savage, D Cowley, et al.
American Journal of Medical Genetics|July 12, 1996
Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardationA K Gedeon, I A Glass, J M Connor, et al.
American Journal of Medical Genetics|April 1, 1992
XLMR genes: update 1992G Neri, P Chiurazzi, F Arena, et al.
Clinical Genetics|June 14, 2000
Mild phenotype in two siblings with distal monosomy 12p13.31-->pterI A Glass, A Trenholme, L Mildenhall, et al.
Journal of Medical Genetics|February 1, 1989
Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenaseI A Glass, C A Swindlehurst, D A Aitken, et al.
Seminars in Liver Disease|March 28, 1998
Molecular genetics of congenital erythropoietic porphyriaR J Desnick, I A Glass, W Xu, et al.
Pageof 5