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Implementation Science : IS|May 1, 2015
Early ART initiation among HIV-positive pregnant women in central Mozambique: a stepped wedge randomized controlled trial of an optimized Option B+ approachJames F Cowan, Mark Micek, Jessica F Greenberg Cowan, et al.
American Journal of Human Genetics|August 11, 1991
Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15J Wagstaff, J H Knoll, J Fleming, et al.
American Journal of Medical Genetics|July 1, 1986
Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndromeR F Stratton, W B Dobyns, F Greenberg, et al.
American Journal of Human Genetics|January 1, 1995
The human homologue of the Drosophila melanogaster flightless-I gene (flil) maps within the Smith-Magenis microdeletion critical region in 17p11.2K S Chen, P H Gunaratne, J D Hoheisel, et al.
Human Genetics|May 1, 1996
Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1 neuropathyB B Roa, F Greenberg, P Gunaratne, et al.
Genomics|July 1, 1992
Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17pV Guzzetta, B Franco, B J Trask, et al.
American Journal of Medical Genetics|September 11, 1995
Smith-Magenis syndrome deletion: a case with equivocal cytogenetic findings resolved by fluorescence in situ hybridizationR C Juyal, F Greenberg, G A Mengden, et al.
American Journal of Human Genetics|December 1, 1991
Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2)F Greenberg, V Guzzetta, R Montes de Oca-Luna, et al.
American Journal of Medical Genetics|March 29, 1996
Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)F Greenberg, R A Lewis, L Potocki, et al.
Human Molecular Genetics|April 1, 1997
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brainM E Ross, K M Allen, A K Srivastava, et al.
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