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American Journal of Medical Genetics
|
December 1, 1984
Are the occasional aneuploid cells in peripheral blood cultures significant?
S L Wenger, W L Golden, S P Dennis, et al.
American Journal of Medical Genetics
|
April 1, 1992
Genetic analyses on a set of parasitic conjoined twins
M W Steele, S L Wenger, R Deka, et al.
American Journal of Medical Genetics
|
November 1, 1988
Case of Pallister-Killian syndrome with imperforate anus
A E Lin, M Clemens, K L Garver, et al.
Clinical Genetics
|
November 1, 1977
Meiotic consequences of an intrachromosomal insertion of chromosome No 1: a family pedigree
S F Pan, S R Fatora, R Sorg, et al.
The Journal of Pediatrics
|
October 1, 1996
A simplified six-item checklist for screening for fragile X syndrome in the pediatric population
C A Giangreco, M W Steele, C E Aston, et al.
American Journal of Medical Genetics
|
October 1, 1992
Acrometageria: a spectrum of "premature aging" syndromes
J M Greally, L Y Boone, S G Lenkey, et al.
American Journal of Medical Genetics
|
August 1, 1992
X inactivation and dystrophin studies in a t(X;12) female: evidence for biochemical normalization in Duchenne muscular dystrophy carriers
S L Wenger, M W Steele, E P Hoffman, et al.
American Journal of Medical Genetics
|
December 1, 1987
Clinical comparison of 59 Prader-Willi patients with and without the 15(q12) deletion
S L Wenger, J M Hanchett, M W Steele, et al.
The Journal of Pediatrics
|
November 1, 1970
The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-)
W R Breg, M W Steele, O J Miller, et al.
American Journal of Medical Genetics
|
January 2, 1995
"Balanced" karyotypes in six abnormal offspring of balanced reciprocal translocation normal carrier parents
S L Wenger, M W Steele, L Y Boone, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 68) with videos related to
Sort By:
Page
of 7
American Journal of Medical Genetics
|
December 1, 1984
Are the occasional aneuploid cells in peripheral blood cultures significant?
S L Wenger, W L Golden, S P Dennis, et al.
American Journal of Medical Genetics
|
April 1, 1992
Genetic analyses on a set of parasitic conjoined twins
M W Steele, S L Wenger, R Deka, et al.
American Journal of Medical Genetics
|
November 1, 1988
Case of Pallister-Killian syndrome with imperforate anus
A E Lin, M Clemens, K L Garver, et al.
Clinical Genetics
|
November 1, 1977
Meiotic consequences of an intrachromosomal insertion of chromosome No 1: a family pedigree
S F Pan, S R Fatora, R Sorg, et al.
The Journal of Pediatrics
|
October 1, 1996
A simplified six-item checklist for screening for fragile X syndrome in the pediatric population
C A Giangreco, M W Steele, C E Aston, et al.
American Journal of Medical Genetics
|
October 1, 1992
Acrometageria: a spectrum of "premature aging" syndromes
J M Greally, L Y Boone, S G Lenkey, et al.
American Journal of Medical Genetics
|
August 1, 1992
X inactivation and dystrophin studies in a t(X;12) female: evidence for biochemical normalization in Duchenne muscular dystrophy carriers
S L Wenger, M W Steele, E P Hoffman, et al.
American Journal of Medical Genetics
|
December 1, 1987
Clinical comparison of 59 Prader-Willi patients with and without the 15(q12) deletion
S L Wenger, J M Hanchett, M W Steele, et al.
The Journal of Pediatrics
|
November 1, 1970
The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-)
W R Breg, M W Steele, O J Miller, et al.
American Journal of Medical Genetics
|
January 2, 1995
"Balanced" karyotypes in six abnormal offspring of balanced reciprocal translocation normal carrier parents
S L Wenger, M W Steele, L Y Boone, et al.
Page
of 7