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American Journal of Medical Genetics
|
May 1, 1988
FG syndrome update 1988: note of 5 new patients and bibliography
J M Opitz, A Richieri-da Costa, J M Aase, et al.
Lancet (London, England)
|
February 2, 1974
Letter: Immunodeficiency in the cerebro-hepato-renal syndrome of Zellweger
K W Gilkrist, J M Opitz, E F Gilbert, et al.
Pediatrics
|
April 1, 1973
X-linked aqueductal stenosis: clinical and neuropathological findings in two families
L B Holmes, A Nash, G M ZuRhein, et al.
Clinical Dysmorphology
|
January 29, 2000
Wolf-Hirschhorn syndrome (WHS): a history in pictures
A Battaglia, J C Carey, D H Viskochil, et al.
American Journal of Medical Genetics
|
January 20, 1997
Autosomal dominant and sporadic radio-ulnar synostosis
R Rizzo, V Pavone, G Corsello, et al.
American Journal of Medical Genetics
|
January 1, 1978
An unusual dysplasia-malformation-cancer syndrome in two patients
M V Durkin-Stamm, E F Gilbert, D J Ganick, et al.
Birth Defects Original Article Series
|
January 1, 1974
Arthrodentoosteodysplasia: a genetic "acroosteolysis" syndrome
F T Zugibe, J Herrmann, J M Opitz, et al.
Lancet (London, England)
|
February 21, 1976
Letter: Trisomy-20 syndrome in man
P D Pallister, J Herrmann, L F Meisner, et al.
American Journal of Medical Genetics
|
March 1, 1987
Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studies
J M Opitz, J W Spranger, H R Stöss, et al.
American Journal of Medical Genetics
|
June 8, 2001
Human anotocephaly (aprosopus, acrania-synotia) in the Vilnius anatomical collection
A Utkus, R Kazakevicius, R Ptasekas, et al.
Page
of 34
Search research articles
Search
Showing results (231-240 of 338) with videos related to
Sort By:
Page
of 34
American Journal of Medical Genetics
|
May 1, 1988
FG syndrome update 1988: note of 5 new patients and bibliography
J M Opitz, A Richieri-da Costa, J M Aase, et al.
Lancet (London, England)
|
February 2, 1974
Letter: Immunodeficiency in the cerebro-hepato-renal syndrome of Zellweger
K W Gilkrist, J M Opitz, E F Gilbert, et al.
Pediatrics
|
April 1, 1973
X-linked aqueductal stenosis: clinical and neuropathological findings in two families
L B Holmes, A Nash, G M ZuRhein, et al.
Clinical Dysmorphology
|
January 29, 2000
Wolf-Hirschhorn syndrome (WHS): a history in pictures
A Battaglia, J C Carey, D H Viskochil, et al.
American Journal of Medical Genetics
|
January 20, 1997
Autosomal dominant and sporadic radio-ulnar synostosis
R Rizzo, V Pavone, G Corsello, et al.
American Journal of Medical Genetics
|
January 1, 1978
An unusual dysplasia-malformation-cancer syndrome in two patients
M V Durkin-Stamm, E F Gilbert, D J Ganick, et al.
Birth Defects Original Article Series
|
January 1, 1974
Arthrodentoosteodysplasia: a genetic "acroosteolysis" syndrome
F T Zugibe, J Herrmann, J M Opitz, et al.
Lancet (London, England)
|
February 21, 1976
Letter: Trisomy-20 syndrome in man
P D Pallister, J Herrmann, L F Meisner, et al.
American Journal of Medical Genetics
|
March 1, 1987
Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studies
J M Opitz, J W Spranger, H R Stöss, et al.
American Journal of Medical Genetics
|
June 8, 2001
Human anotocephaly (aprosopus, acrania-synotia) in the Vilnius anatomical collection
A Utkus, R Kazakevicius, R Ptasekas, et al.
Page
of 34