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Blood|November 15, 1993
Trisomy 21 in childhood acute lymphoblastic leukemia: a Pediatric Oncology Group study (8602)M S Watson, A J Carroll, J J Shuster, et al.
The American Journal of Cardiology|July 1, 1995
Deletion within chromosome 22 is common in patients with absent pulmonary valve syndromeM C Johnson, A W Strauss, S B Dowton, et al.
American Journal of Human Genetics|August 2, 2007
A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGINK Lehmann, P Seemann, F Silan, et al.
The New England Journal of Medicine|March 9, 1989
The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalitiesG G Rhoads, L G Jackson, S E Schlesselman, et al.
The Journal of Rural Health : Official Journal of the American Rural Health Association and the National Rural Health Care Association|April 11, 2026
Rural health care workforce retention measures: A rapid scoping reviewMichelle A Mengeling, Rachel Sears, Casey H Buchanan, et al.
Ecological Applications : a Publication of the Ecological Society of America|January 5, 2017
Ecosystem carbon density and allocation across a chronosequence of longleaf pine forestsLisa J Samuelson, Thomas A Stokes, John R Butnor, et al.
Health Technology Assessment (Winchester, England)|February 8, 2005
Improving the referral process for familial breast cancer genetic counselling: findings of three randomised controlled trials of two interventionsB J Wilson, N Torrance, J Mollison, et al.
The Journal of Clinical Investigation|December 10, 1999
Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathwaysD W Benson, G M Silberbach, A Kavanaugh-McHugh, et al.
Science (New York, N.Y.)|April 10, 2004
Quantifying stratospheric ozone in the upper troposphere with in situ measurements of HClT P Marcy, D W Fahey, R S Gao, et al.
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