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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
|
May 1, 1988
Experience with multiple approaches to the prenatal diagnosis of the fragile X syndrome: amniotic fluid, chorionic villi, fetal blood and molecular methods
L R Shapiro, P L Wilmot, P D Murphy, et al.
The Journal of Pediatrics
|
July 1, 1971
Trisomy 22: a clinical entity
L Y Hsu, L R Shapiro, M Gertner, et al.
The American Journal of Clinical Nutrition
|
December 1, 1981
Body composition and physical activity in 8-year-old children
L C Ku, L R Shapiro, P B Crawford, et al.
Birth Defects Original Article Series
|
January 1, 1974
The human simian crease and its variants. A model for investigation of serious congenital malformation
E B Hook, R Bonenfant, M L Powers, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
September 1, 1986
Increased echogenicity in the lower fetal abdomen: a common normal variant in the second trimester
J Fakhry, M Reiser, L R Shapiro, et al.
American Journal of Diseases of Children (1960)
|
August 1, 1971
Deceleration of intellectual development in a XXXXY child: a follow-up
L R Shapiro, C B Brill, L Y Hsu, 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.
Obstetrics and Gynecology
|
November 1, 1970
Parental chromosomal aberrations associated with multiple abortions and an abnormal infant
L Y Hsu, M Barcinski, L R Shapiro, et al.
Obstetrical & Gynecological Survey
|
March 1, 1978
Amniocentesis for prenatal diagnosis
A Chervin, P B Farnsworth, W L Freedman, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 98) with videos related to
Sort By:
Page
of 10
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
|
May 1, 1988
Experience with multiple approaches to the prenatal diagnosis of the fragile X syndrome: amniotic fluid, chorionic villi, fetal blood and molecular methods
L R Shapiro, P L Wilmot, P D Murphy, et al.
The Journal of Pediatrics
|
July 1, 1971
Trisomy 22: a clinical entity
L Y Hsu, L R Shapiro, M Gertner, et al.
The American Journal of Clinical Nutrition
|
December 1, 1981
Body composition and physical activity in 8-year-old children
L C Ku, L R Shapiro, P B Crawford, et al.
Birth Defects Original Article Series
|
January 1, 1974
The human simian crease and its variants. A model for investigation of serious congenital malformation
E B Hook, R Bonenfant, M L Powers, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
September 1, 1986
Increased echogenicity in the lower fetal abdomen: a common normal variant in the second trimester
J Fakhry, M Reiser, L R Shapiro, et al.
American Journal of Diseases of Children (1960)
|
August 1, 1971
Deceleration of intellectual development in a XXXXY child: a follow-up
L R Shapiro, C B Brill, L Y Hsu, 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.
Obstetrics and Gynecology
|
November 1, 1970
Parental chromosomal aberrations associated with multiple abortions and an abnormal infant
L Y Hsu, M Barcinski, L R Shapiro, et al.
Obstetrical & Gynecological Survey
|
March 1, 1978
Amniocentesis for prenatal diagnosis
A Chervin, P B Farnsworth, W L Freedman, et al.
Page
of 10