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J W Pierpont

Showing results (1-10 of 6) with videos related to

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American Journal of Human Genetics|March 1, 1993
Facts on PAXJ W Pierpont, R P Erickson
Clinical Genetics|March 1, 1995
A family with unusual Waardenburg syndrome type I (WSI), cleft lip (palate), and Hirschsprung disease is not linked to PAX 3J W Pierpont, D St Jacques, L H Seaver, et al.
Clinical Genetics|December 1, 1996
Size of 22q deletions in four previously reported patients with conotruncal anomaly face syndromeJ W Pierpont, R P Erickson, F H Thompson, et al.
Human Mutation|January 1, 1994
A single base pair substitution within the paired box of PAX3 in an individual with Waardenburg syndrome type 1 (WS1)J W Pierpont, L D Doolan, K Amann, et al.
Journal of Medical Genetics|November 1, 1994
Pulmonary atresia associated with maternal 22q11.2 deletion: possible parent of origin effect in the conotruncal anomaly face syndromeL H Seaver, J W Pierpont, R P Erickson, et al.
Journal of Craniofacial Genetics and Developmental Biology|April 1, 1995
Lack of linkage of apparently dominant cleft lip (palate) to two candidate chromosomal regionsJ W Pierpont, A L Storm, R P Erickson, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
American Journal of Human Genetics|March 1, 1993
Facts on PAXJ W Pierpont, R P Erickson
Clinical Genetics|March 1, 1995
A family with unusual Waardenburg syndrome type I (WSI), cleft lip (palate), and Hirschsprung disease is not linked to PAX 3J W Pierpont, D St Jacques, L H Seaver, et al.
Clinical Genetics|December 1, 1996
Size of 22q deletions in four previously reported patients with conotruncal anomaly face syndromeJ W Pierpont, R P Erickson, F H Thompson, et al.
Human Mutation|January 1, 1994
A single base pair substitution within the paired box of PAX3 in an individual with Waardenburg syndrome type 1 (WS1)J W Pierpont, L D Doolan, K Amann, et al.
Journal of Medical Genetics|November 1, 1994
Pulmonary atresia associated with maternal 22q11.2 deletion: possible parent of origin effect in the conotruncal anomaly face syndromeL H Seaver, J W Pierpont, R P Erickson, et al.
Journal of Craniofacial Genetics and Developmental Biology|April 1, 1995
Lack of linkage of apparently dominant cleft lip (palate) to two candidate chromosomal regionsJ W Pierpont, A L Storm, R P Erickson, et al.
Pageof 1