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D D Weaver

Showing results (71-80 of 99) with videos related to

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American Journal of Medical Genetics|January 1, 1981
Cartilage-hair hypoplasia, defective T-cell function, and Diamond-Blackfan anemia in an Amish childR E Harris, R L Baehner, S Gleiser, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1990
A morphometric analysis of the fetal craniofacies by ultrasound: fetal cephalometryL F Escobar, D Bixler, L M Padilla, et al.
American Journal of Medical Genetics|August 15, 1994
Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotypeR Mewar, W Harrison, D D Weaver, et al.
American Journal of Medical Genetics|October 1, 1983
Hirschsprung disease: etiologic implications of unsuccessful prenatal diagnosisA L Jarmas, D D Weaver, L M Padilla, et al.
The Journal of Pediatrics|June 1, 1983
Juvenile chronic granulocytic leukemia in a patient with trisomy 8, neurofibromatosis, and prolonged Epstein-Barr virus infectionC G Palmer, A J Provisor, D D Weaver, et al.
American Journal of Medical Genetics|May 1, 1982
Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:)R S Young, C G Palmer, H A Bender, et al.
The Journal of Urology|January 23, 1999
Genitourinary anomalies in the CHARGE associationD C Ragan, A J Casale, R C Rink, et al.
The Journal of Clinical Investigation|April 1, 1984
A mutation that causes lability of the androgen receptor under conditions that normally promote transformation to the DNA-binding stateW J Kovacs, J E Griffin, D D Weaver, et al.
Clinical Genetics|August 1, 1988
Neural tube defects and omphalocele in trisomy 18C A Moore, J P Harmon, L M Padilla, et al.
Plastic and Reconstructive Surgery|September 1, 1990
Unilateral duplication of the cerebellar hemisphere and internal, middle, and external ear: a clinical case studyJ M Jackson, A M Sadove, D D Weaver, et al.
Pageof 10

Showing results (71-80 of 99) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics|January 1, 1981
Cartilage-hair hypoplasia, defective T-cell function, and Diamond-Blackfan anemia in an Amish childR E Harris, R L Baehner, S Gleiser, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1990
A morphometric analysis of the fetal craniofacies by ultrasound: fetal cephalometryL F Escobar, D Bixler, L M Padilla, et al.
American Journal of Medical Genetics|August 15, 1994
Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotypeR Mewar, W Harrison, D D Weaver, et al.
American Journal of Medical Genetics|October 1, 1983
Hirschsprung disease: etiologic implications of unsuccessful prenatal diagnosisA L Jarmas, D D Weaver, L M Padilla, et al.
The Journal of Pediatrics|June 1, 1983
Juvenile chronic granulocytic leukemia in a patient with trisomy 8, neurofibromatosis, and prolonged Epstein-Barr virus infectionC G Palmer, A J Provisor, D D Weaver, et al.
American Journal of Medical Genetics|May 1, 1982
Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:)R S Young, C G Palmer, H A Bender, et al.
The Journal of Urology|January 23, 1999
Genitourinary anomalies in the CHARGE associationD C Ragan, A J Casale, R C Rink, et al.
The Journal of Clinical Investigation|April 1, 1984
A mutation that causes lability of the androgen receptor under conditions that normally promote transformation to the DNA-binding stateW J Kovacs, J E Griffin, D D Weaver, et al.
Clinical Genetics|August 1, 1988
Neural tube defects and omphalocele in trisomy 18C A Moore, J P Harmon, L M Padilla, et al.
Plastic and Reconstructive Surgery|September 1, 1990
Unilateral duplication of the cerebellar hemisphere and internal, middle, and external ear: a clinical case studyJ M Jackson, A M Sadove, D D Weaver, et al.
Pageof 10