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American Journal of Medical Genetics|September 1, 1993
Reproductive failure in a patient with neurofibromatosis-Noonan syndromeD Meschede, U G Froster, F Gullotta, et al.
Klinische Wochenschrift|November 2, 1982
Minicore myopathyF Gullotta, L Pavone, M La Rosa, et al.
American Journal of Medical Genetics|January 1, 1988
Skeletal anomalies in trisomy 21 as an example of amplified developmental instability in chromosome disorders: a histological study of the feet of 21 mid-trimester fetuses with trisomy 21E Blum-Hoffmann, H Rehder, U Langenbeck
Der Urologe. Ausg. A|July 1, 1975
[XX-male-syndrome. Pathogenesis and aspects of diagnostic pitfalls (author's transl)]H Rehder, P Brühl, P K Seth
Teratology|April 1, 1982
Fetal manifestation of a chromosomal disorder: partial duplication of the long arm of chromosome 5 (5q33 to qter)E Passarge, M Bartsch-Sandhoff, H Rehder
Der Nervenarzt|May 1, 1993
[Schizophreniform psychosis in paraneoplastic limbic encephalitis]J Frommer, A Haass, M Bergmann, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1978
Schwartz-Jampel syndrome in two daughters of first cousinsL Pavone, F Mollica, A Grasso, et al.
Der Pathologe|September 1, 1995
[Neurocysticercosis]G Roos, T Henze, F Gullotta, et al.
Neuropathology and Applied Neurobiology|April 1, 1993
Heterogeneity of centronuclear myopathy shown by flow cytometry of nuclear DNAK Metze, R Schnabel, W Mellin, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|May 26, 1998
Oligodendrocyte and axon pathology in clinically silent multiple sclerosis lesionsI Mews, M Bergmann, S Bunkowski, et al.
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