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E K Pivnick

Showing results (1-10 of 24) with videos related to

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Journal of Medical Genetics|October 23, 1998
Neurofibromatosis type 1 (NF1): a protein truncation assay yielding identification of mutations in 73% of patientsV M Park, E K Pivnick
Journal of Medical Genetics|August 27, 1998
Bony orbital morphology in neurofibromatosis type 1 (NF1)S C Kaste, E K Pivnick
Clinical Dysmorphology|April 20, 2001
Long-term survival in Patau syndromeY Tunca, J S Kadandale, E K Pivnick
Journal of Medical Genetics|August 1, 1996
Gorlin syndrome associated with midline nasal dermoid cystE K Pivnick, A W Walter, M D Lawrence, et al.
Pediatric Dermatology|May 1, 1997
Hair whorl as an indicator of a mediastinal plexiform neurofibromaE K Pivnick, T E Lobe, S J Fitch, et al.
Human Genetics|December 18, 1998
Alternative splicing of exons 29 and 30 in the neurofibromatosis type 1 geneV M Park, K A Kenwright, D B Sturtevant, et al.
Journal of Pediatric Hematology/Oncology|May 1, 1997
Complications of the nevoid basal cell carcinoma syndrome: a case reportA W Walter, E K Pivnick, A E Bale, et al.
Human Genetics|November 1, 1992
Mutations in the conserved domain of SRY are uncommon in XY gonadal dysgenesisE K Pivnick, S Wachtel, D Woods, et al.
American Journal of Medical Genetics|December 15, 1991
Hallermann-Streiff syndrome with hypopituitarism contributing to growth failureE K Pivnick, S Burstein, R S Wilroy, et al.
Teratology|December 5, 1998
Infant with midline thoracoabdominal schisis and limb defectsE K Pivnick, R A Kaufman, G V Velagaleti, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|October 23, 1998
Neurofibromatosis type 1 (NF1): a protein truncation assay yielding identification of mutations in 73% of patientsV M Park, E K Pivnick
Journal of Medical Genetics|August 27, 1998
Bony orbital morphology in neurofibromatosis type 1 (NF1)S C Kaste, E K Pivnick
Clinical Dysmorphology|April 20, 2001
Long-term survival in Patau syndromeY Tunca, J S Kadandale, E K Pivnick
Journal of Medical Genetics|August 1, 1996
Gorlin syndrome associated with midline nasal dermoid cystE K Pivnick, A W Walter, M D Lawrence, et al.
Pediatric Dermatology|May 1, 1997
Hair whorl as an indicator of a mediastinal plexiform neurofibromaE K Pivnick, T E Lobe, S J Fitch, et al.
Human Genetics|December 18, 1998
Alternative splicing of exons 29 and 30 in the neurofibromatosis type 1 geneV M Park, K A Kenwright, D B Sturtevant, et al.
Journal of Pediatric Hematology/Oncology|May 1, 1997
Complications of the nevoid basal cell carcinoma syndrome: a case reportA W Walter, E K Pivnick, A E Bale, et al.
Human Genetics|November 1, 1992
Mutations in the conserved domain of SRY are uncommon in XY gonadal dysgenesisE K Pivnick, S Wachtel, D Woods, et al.
American Journal of Medical Genetics|December 15, 1991
Hallermann-Streiff syndrome with hypopituitarism contributing to growth failureE K Pivnick, S Burstein, R S Wilroy, et al.
Teratology|December 5, 1998
Infant with midline thoracoabdominal schisis and limb defectsE K Pivnick, R A Kaufman, G V Velagaleti, et al.
Pageof 3