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Prenatal Diagnosis|March 1, 1984
Evaluation of inorganic pyrophosphate in amniotic fluid as a mode of prenatal diagnosis of osteogenesis imperfectaK L Garver, M G Blitzer, G Ibezim, et al.Journal of Medical Genetics|November 1, 1988
Chromosome subband 17p11.2 deletion: a minute deletion syndromeD Lockwood, F Hecht, C Dowman, et al.Clinical Genetics|October 23, 2009
Noonan syndrome and neurofibromatosis type I in a family with a novel mutation in NF1A M Nyström, S Ekvall, J Allanson, et al.Familial Cancer|September 5, 2013
Reflex testing for Lynch syndrome: if we build it, will they come? Lessons learned from the uptake of clinical genetics services by individuals with newly diagnosed colorectal cancer (CRC)E Tomiak, A Samson, N Spector, et al.Human Molecular Genetics|August 1, 1994
Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22E G Puffenberger, E R Kauffman, S Bolk, et al.Clinical Genetics|April 29, 2005
Psychological and genetic counseling implications for adolescent daughters of mothers with breast cancerM Cappelli, S Verma, Y Korneluk, et al.CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|November 1, 1993
Recommendations on the use of folic acid supplementation to prevent the recurrence of neural tube defects. Clinical Teratology Committee, Canadian College of Medical GeneticistsM I Van Allen, F C Fraser, L Dallaire, et al.Journal of Medical Genetics|July 11, 2006
The cardiofaciocutaneous syndromeA Roberts, J Allanson, S K Jadico, et al.American Journal of Medical Genetics|November 15, 1993
Familial Brachmann-de Lange syndrome: further evidence for autosomal dominant inheritance and review of the literatureM Feingold, A E LinPageof 9