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Teratology
|
December 1, 1987
TC-83 Venezuelan equine encephalitis vaccine exposure during pregnancy
A C Casamassima, L W Hess, A Marty
Clinical Genetics
|
August 1, 1990
Disomic balanced reciprocal translocation
P L Wilmot, L R Shapiro, A C Casamassima
American Journal of Medical Genetics
|
August 1, 1987
Wrinkly skin syndrome: phenotype and additional manifestations
A C Casamassima, S K Wesson, C J Conlon, et al.
American Journal of Medical Genetics
|
February 1, 1987
A new syndrome with features of the Smith-Lemli-Opitz and Meckel-Gruber syndromes in a sibship with cerebellar defects
A C Casamassima, P Mamunes, I M Gladstone, et al.
Clinical Genetics
|
April 1, 1991
Prader-Willi syndrome and Robertsonian translocations involving chromosome 15
A C Casamassima, L R Shapiro, P L Wilmot, et al.
American Journal of Medical Genetics
|
March 1, 1993
Kallmann syndrome associated with complex chromosome rearrangement
A C Casamassima, P L Wilmot, B K Vibert, et al.
American Journal of Medical Genetics
|
December 1, 1990
Deletion of 16q with prolonged survival and unusual radiographic manifestations
A C Casamassima, R M Klein, P L Wilmot, et al.
Neurology
|
August 1, 1988
Multiple sulfatase deficiency
B W Soong, A C Casamassima, J K Fink, et al.
Clinical Genetics
|
April 1, 1989
Trisomy 5 mosaicism in amniotic fluid with normal outcome
A C Casamassima, P L Wilmot, M J Mahoney, et al.
American Journal of Medical Genetics
|
February 1, 1991
Cytogenetic diagnosis of the fragile X syndrome: efficiency, utilization, and trends
L R Shapiro, P L Wilmot, D A Shapiro, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
Teratology
|
December 1, 1987
TC-83 Venezuelan equine encephalitis vaccine exposure during pregnancy
A C Casamassima, L W Hess, A Marty
Clinical Genetics
|
August 1, 1990
Disomic balanced reciprocal translocation
P L Wilmot, L R Shapiro, A C Casamassima
American Journal of Medical Genetics
|
August 1, 1987
Wrinkly skin syndrome: phenotype and additional manifestations
A C Casamassima, S K Wesson, C J Conlon, et al.
American Journal of Medical Genetics
|
February 1, 1987
A new syndrome with features of the Smith-Lemli-Opitz and Meckel-Gruber syndromes in a sibship with cerebellar defects
A C Casamassima, P Mamunes, I M Gladstone, et al.
Clinical Genetics
|
April 1, 1991
Prader-Willi syndrome and Robertsonian translocations involving chromosome 15
A C Casamassima, L R Shapiro, P L Wilmot, et al.
American Journal of Medical Genetics
|
March 1, 1993
Kallmann syndrome associated with complex chromosome rearrangement
A C Casamassima, P L Wilmot, B K Vibert, et al.
American Journal of Medical Genetics
|
December 1, 1990
Deletion of 16q with prolonged survival and unusual radiographic manifestations
A C Casamassima, R M Klein, P L Wilmot, et al.
Neurology
|
August 1, 1988
Multiple sulfatase deficiency
B W Soong, A C Casamassima, J K Fink, et al.
Clinical Genetics
|
April 1, 1989
Trisomy 5 mosaicism in amniotic fluid with normal outcome
A C Casamassima, P L Wilmot, M J Mahoney, et al.
American Journal of Medical Genetics
|
February 1, 1991
Cytogenetic diagnosis of the fragile X syndrome: efficiency, utilization, and trends
L R Shapiro, P L Wilmot, D A Shapiro, et al.
Page
of 2