DiGeorge syndrome: an historical review of clinical and cytogenetic features.

Por Greenberg, F
Publicado em 1993

Osteoglophonic dysplasia.

Por Greenberg, F, Lewis, R A
Publicado em 1990

Integration of a rehabilitation center into a metropolitan community.

Por Krause, E. A., Greenberg, F. S.
Publicado em 1967

The face of Smith-Magenis syndrome: a subjective and objective study

Por Allanson, J., Greenberg, F., Smith, A.
Publicado em 1999

Molecular studies of DiGeorge syndrome.

Por Fibison, W J, Budarf, M, McDermid, H, Greenberg, F, Emanuel, B S
Publicado em 1990

Cytogenetic findings in a prospective series of patients with DiGeorge anomaly.

Por Greenberg, F, Elder, F F, Haffner, P, Northrup, H, Ledbetter, D H
Publicado em 1988

Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndrome.

Por Nickerson, E, Greenberg, F, Keating, M T, McCaskill, C, Shaffer, L G
Publicado em 1995

Clinical and molecular evaluation of four patients with partial duplications of the long arm of chromosome 18.

Por Mewar, R, Kline, A D, Harrison, W, Rojas, K, Greenberg, F, Overhauser, J
Publicado em 1993

Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndrome.

Por Elsea, S H, Juyal, R C, Jiralerspong, S, Finucane, B M, Pandolfo, M, Greenberg, F, Baldini, A, Stover, P, Patel, P I
Publicado em 1995

Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients.

Por Juyal, R. C., Figuera, L. E., Hauge, X., Elsea, S. H., Lupski, J. R., Greenberg, F., Baldini, A., Patel, P. I.
Publicado em 1996

Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4.

Por Altherr, M. R., Bengtsson, U., Elder, F. F., Ledbetter, D. H., Wasmuth, J. J., McDonald, M. E., Gusella, J. F., Greenberg, F.
Publicado em 1991

Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.

Por Shapira, S K, McCaskill, C, Northrup, H, Spikes, A S, Elder, F F, Sutton, V R, Korenberg, J R, Greenberg, F, Shaffer, L G
Publicado em 1997

The human homologue of the Drosophila melanogaster flightless-I gene (flil) maps within the Smith-Magenis microdeletion critical region in 17p11.2.

Por Chen, K S, Gunaratne, P H, Hoheisel, J D, Young, I G, Miklos, G L, Greenberg, F, Shaffer, L G, Campbell, H D, Lupski, J R
Publicado em 1995

Localization of the gene encoding the GABAA receptor β3 subunit to the Angelman/Prader-Willi region of human chromosome 15

Por Wagstaff, J., Knoll, J. H. M., Fleming, J., Kirkness, E. F., Martin-Gallardo, A., Greenberg, F., Graham, J. M., Menninger, J., Ward, D., Venter, J. C., Lalande, M.
Publicado em 1991

Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).

Por Greenberg, F, Guzzetta, V, Montes de Oca-Luna, R, Magenis, R E, Smith, A C, Richter, S F, Kondo, I, Dobyns, W B, Patel, P I, Lupski, J R
Publicado em 1991

Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21

Por McGinniss, M. J., Kazazian, H. H., Stetten, G., Petersen, M. B., Boman, H., Engel, E., Greenberg, F., Hertz, J. M., Johnson, A., Laca, Z., Mikkelsen, M., Patil, S. R., Schinzel, A. A., Tranebjaerg, L., Antonarakis, S. E.
Publicado em 1992