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Prenatal Diagnosis|June 1, 1991
Anxiety in women with low maternal serum alpha-fetoprotein screening resultsD N Abuelo, M R Hopmann, G Barsel-Bowers, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 1, 1990
Acute renal insufficiency due to renal infarctions in a patient with neurofibromatosisD A DiPrete, J G Abuelo, D N Abuelo, et al.Journal of Surgical Oncology|October 1, 1988
Ataxia telangiectasia and acinic cell carcinoma of the parotid glandC Mock, G Coleman, J H Ree, et al.American Journal of Medical Genetics|April 10, 1995
Prenatal detection of the cholesterol biosynthetic defect in the Smith-Lemli-Opitz syndrome by the analysis of amniotic fluid sterolsD N Abuelo, G S Tint, R Kelley, et al.JAMA|April 13, 1979
Prenatal diagnosis of homozygous alpha-thalassemiaA M Dozy, E N Forman, D N Abuelo, et al.American Journal of Medical Genetics|July 16, 1999
Ocular anterior chamber dysgenesis in craniosynostosis syndromes with a fibroblast growth factor receptor 2 mutationK Okajima, L K Robinson, M A Hart, et al.The Journal of Pediatrics|July 1, 1995
Correlation of severity and outcome with plasma sterol levels in variants of the Smith-Lemli-Opitz syndromeG S Tint, G Salen, A K Batta, et al.American Journal of Medical Genetics|May 2, 1997
Macrocephaly-cutis marmorata telangiectatica congenita: a distinct disorder with developmental delay and connective tissue abnormalitiesC A Moore, H V Toriello, D N Abuelo, et al.Human Genetics|December 1, 1996
Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patientsB J Trask, H Mefford, G van den Engh, et al.Human Genetics|April 3, 2001
Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosomeM D Mailman, T Hemingway, R L Darsey, et al.Pageof 2