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J T Hecht

Showing results (21-30 of 104) with videos related to

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Nucleic Acids Research|December 11, 1991
TaqI and HaeIII RFLP polymorphisms in human proteoglycan link gene (CRTL1)J T Hecht, Y Wang, C Rhodes, et al.
Nucleic Acids Research|December 11, 1991
GT repeat polymorphism in the human proteoglycan link gene (CRTL1) promoter regionJ T Hecht, Y Wang, C Rhodes, et al.
Prenatal Diagnosis|March 1, 1994
Tibial hemimelia syndrome: prenatal diagnosis by real-time ultrasoundM Ramirez, J T Hecht, S Taylor, et al.
Journal of Medical Genetics|January 1, 1995
Exclusion of retinoic acid receptor and a cartilage matrix protein in non-syndromic CL(P) familiesJ D Stein, J T Hecht, S H Blanton
Journal of Neurosurgery|August 1, 1989
Foramen magnum decompression for homozygous achondroplasiaJ T Hecht, I J Butler, W A Horton
Southern Medical Journal|December 1, 1981
A recognizable syndrome of sex-linked mental retardation, large testes, and marker X chromosomeJ T Hecht, C M Moore, C I Scott
American Journal of Medical Genetics|January 2, 1995
Natural history study of hereditary multiple exostosesC L Wicklund, R M Pauli, D Johnston, et al.
Clinical Genetics|March 21, 2002
Familial case of Potocki-Shaffer syndrome associated with microdeletion of EXT2 and ALX4C R Hall, Y Wu, L G Shaffer, et al.
American Journal of Medical Genetics|March 1, 1993
Familial interstitial deletion 11(p11.12p12) associated with parietal foramina, brachymicrocephaly, and mental retardationL G Shaffer, J T Hecht, D H Ledbetter, et al.
American Journal of Human Genetics|August 1, 1992
Van der Woude syndrome and nonsyndromic cleft lip and palateJ T Hecht, Y Wang, S H Blanton, et al.
Pageof 11

Showing results (21-30 of 104) with videos related to

Sort By:
Pageof 11
Nucleic Acids Research|December 11, 1991
TaqI and HaeIII RFLP polymorphisms in human proteoglycan link gene (CRTL1)J T Hecht, Y Wang, C Rhodes, et al.
Nucleic Acids Research|December 11, 1991
GT repeat polymorphism in the human proteoglycan link gene (CRTL1) promoter regionJ T Hecht, Y Wang, C Rhodes, et al.
Prenatal Diagnosis|March 1, 1994
Tibial hemimelia syndrome: prenatal diagnosis by real-time ultrasoundM Ramirez, J T Hecht, S Taylor, et al.
Journal of Medical Genetics|January 1, 1995
Exclusion of retinoic acid receptor and a cartilage matrix protein in non-syndromic CL(P) familiesJ D Stein, J T Hecht, S H Blanton
Journal of Neurosurgery|August 1, 1989
Foramen magnum decompression for homozygous achondroplasiaJ T Hecht, I J Butler, W A Horton
Southern Medical Journal|December 1, 1981
A recognizable syndrome of sex-linked mental retardation, large testes, and marker X chromosomeJ T Hecht, C M Moore, C I Scott
American Journal of Medical Genetics|January 2, 1995
Natural history study of hereditary multiple exostosesC L Wicklund, R M Pauli, D Johnston, et al.
Clinical Genetics|March 21, 2002
Familial case of Potocki-Shaffer syndrome associated with microdeletion of EXT2 and ALX4C R Hall, Y Wu, L G Shaffer, et al.
American Journal of Medical Genetics|March 1, 1993
Familial interstitial deletion 11(p11.12p12) associated with parietal foramina, brachymicrocephaly, and mental retardationL G Shaffer, J T Hecht, D H Ledbetter, et al.
American Journal of Human Genetics|August 1, 1992
Van der Woude syndrome and nonsyndromic cleft lip and palateJ T Hecht, Y Wang, S H Blanton, et al.
Pageof 11