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Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 1, 1994
Mapping of the ACTH, MSH, and neural (MC3 and MC4) melanocortin receptors in the mouse and humanR E Magenis, L Smith, J H Nadeau, et al.American Journal of Human Genetics|November 1, 1990
A human D1 dopamine receptor gene is located on chromosome 5 at q35.1 and identifies an EcoRI RFLPD K Grandy, Q Y Zhou, L Allen, et al.Prenatal Diagnosis|October 1, 1987
Fetal karyotype following ascertainment of fetal anomalies by ultrasoundC G Palmer, J H Miles, P N Howard-Peebles, et al.American Journal of Medical Genetics|May 1, 1990
Aland Island eye disease (Forsius-Eriksson ocular albinism) and an Xp21 deletion in a patient with Duchenne muscular dystrophy, glycerol kinase deficiency, and congenital adrenal hypoplasiaD A Pillers, R G Weleber, B R Powell, et al.Human Genetics|May 1, 1987
A hypervariable region at the D19S11 locusN E Buroker, L Bufton, U Surti, et al.American Journal of Diseases of Children (1960)|October 1, 1990
Transient myeloproliferative disorder of the Down type in the normal newbornD Ridgway, G I Benda, E Magenis, et al.Nucleic Acids Research|June 11, 1990
Characterization and organization of DNA sequences adjacent to the human telomere associated repeat (TTAGGG)nB Weber, C Collins, C Robbins, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|August 1, 1989
Aland Island eye disease (Forsius-Eriksson syndrome) associated with contiguous deletion syndrome at Xp21. Similarity to incomplete congenital stationary night blindnessR G Weleber, D A Pillers, B R Powell, et al.The British Journal of Educational Psychology|June 1, 1992
Shyness and education: the relationship between shyness, social class and personality variables in adolescentsB Lawrence, S BennettPageof 228