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American Journal of Medical Genetics
|
January 1, 1984
5-azacytidine decreases the frequency of fragile X expression in peripheral lymphocyte culture
V G Dev, C Mixon
American Journal of Medical Genetics
|
October 23, 1997
Direct karyotyping of unstimulated newborn blood: a rapid diagnostic method for the clinical management of critically ill newborns
S A Tharapel, V G Dev
American Journal of Human Genetics
|
November 1, 1983
Fragile X expression is decreased by 5-azacytidine and S-adenosylhomocysteine
J C Mixon, V G Dev
Indian Journal of Pediatrics
|
July 1, 1986
Fragile X syndrome: clinical, cytogenetic, biochemical and molecular features
J C Mixon, V G Dev
American Journal of Human Genetics
|
April 1, 1989
Dystrophin: what is in the name?
T A Hurlbut, V G Dev
American Journal of Medical Genetics
|
July 3, 1995
Pallister-Killian syndrome detected by fluorescence in situ hybridization
M G Bulter, V G Dev
The Alabama Journal of Medical Sciences
|
July 1, 1984
Understanding the fragile X syndrome
J C Mixon, V G Dev
Human Genetics
|
October 2, 1979
Partial translocation of NOR and its activity in a balanced carrier and in her cri-du-chat fetus
V G Dev, J Byrne, G Bunch
Human Genetics
|
January 1, 1984
Yqs in an American family of Scottish descent
K Iinuma, W Wertelecki, V G Dev
Prenatal Diagnosis
|
December 18, 2001
Familial X centromere variant resulting in false-positive prenatal diagnosis of monosomy X by interphase FISH
K Tsuchiya, M G Schueler, V G Dev
Page
of 8
Search research articles
Search
Showing results (1-10 of 72) with videos related to
Sort By:
Page
of 8
American Journal of Medical Genetics
|
January 1, 1984
5-azacytidine decreases the frequency of fragile X expression in peripheral lymphocyte culture
V G Dev, C Mixon
American Journal of Medical Genetics
|
October 23, 1997
Direct karyotyping of unstimulated newborn blood: a rapid diagnostic method for the clinical management of critically ill newborns
S A Tharapel, V G Dev
American Journal of Human Genetics
|
November 1, 1983
Fragile X expression is decreased by 5-azacytidine and S-adenosylhomocysteine
J C Mixon, V G Dev
Indian Journal of Pediatrics
|
July 1, 1986
Fragile X syndrome: clinical, cytogenetic, biochemical and molecular features
J C Mixon, V G Dev
American Journal of Human Genetics
|
April 1, 1989
Dystrophin: what is in the name?
T A Hurlbut, V G Dev
American Journal of Medical Genetics
|
July 3, 1995
Pallister-Killian syndrome detected by fluorescence in situ hybridization
M G Bulter, V G Dev
The Alabama Journal of Medical Sciences
|
July 1, 1984
Understanding the fragile X syndrome
J C Mixon, V G Dev
Human Genetics
|
October 2, 1979
Partial translocation of NOR and its activity in a balanced carrier and in her cri-du-chat fetus
V G Dev, J Byrne, G Bunch
Human Genetics
|
January 1, 1984
Yqs in an American family of Scottish descent
K Iinuma, W Wertelecki, V G Dev
Prenatal Diagnosis
|
December 18, 2001
Familial X centromere variant resulting in false-positive prenatal diagnosis of monosomy X by interphase FISH
K Tsuchiya, M G Schueler, V G Dev
Page
of 8