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J A Bartley

Showing results (1-10 of 13) with videos related to

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Pediatric Research|March 1, 1985
Glycerol kinase deficiency inhibits glycerol utilization in phosphoglyceride and triacylglycerol biosynthesisJ A Bartley, R Ward
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1988
Microcephaly in familial holoprosencephalyH H Ardinger, J A Bartley
Ophthalmology|June 1, 1989
X-linked progressive cone dystrophy. Clinical characteristics of affected males and female carriersD M Jacobson, H S Thompson, J A Bartley
The Journal of Pediatrics|February 1, 1986
Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletionJ A Bartley, S Patil, S Davenport, et al.
The Journal of Pediatrics|June 1, 1983
Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndromeM Waziri, S R Patil, J W Hanson, et al.
Clinical Genetics|May 1, 1977
Prenatal diagnosis of dysplastic kidney diseaseJ A Bartley, M S Golbus, R A Filly, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 1, 1984
Orbital hypotelorism. An isolated autosomal dominant traitG F Judisch, S P Kraft, J A Bartley, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|February 1, 1996
Fluconazole-induced congenital anomalies in three infantsT J Pursley, I K Blomquist, J Abraham, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 1, 1994
Ocular findings associated with a Cys39Arg mutation in the Norrie disease geneK M Joos, A E Kimura, K Vandenburgh, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|August 28, 2001
Analysis of speech characteristics in children with velocardiofacial syndrome (VCFS) and children with phenotypic overlap without VCFSL L D'Antonio, N J Scherer, L L Miller, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Pediatric Research|March 1, 1985
Glycerol kinase deficiency inhibits glycerol utilization in phosphoglyceride and triacylglycerol biosynthesisJ A Bartley, R Ward
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1988
Microcephaly in familial holoprosencephalyH H Ardinger, J A Bartley
Ophthalmology|June 1, 1989
X-linked progressive cone dystrophy. Clinical characteristics of affected males and female carriersD M Jacobson, H S Thompson, J A Bartley
The Journal of Pediatrics|February 1, 1986
Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletionJ A Bartley, S Patil, S Davenport, et al.
The Journal of Pediatrics|June 1, 1983
Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndromeM Waziri, S R Patil, J W Hanson, et al.
Clinical Genetics|May 1, 1977
Prenatal diagnosis of dysplastic kidney diseaseJ A Bartley, M S Golbus, R A Filly, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 1, 1984
Orbital hypotelorism. An isolated autosomal dominant traitG F Judisch, S P Kraft, J A Bartley, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|February 1, 1996
Fluconazole-induced congenital anomalies in three infantsT J Pursley, I K Blomquist, J Abraham, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 1, 1994
Ocular findings associated with a Cys39Arg mutation in the Norrie disease geneK M Joos, A E Kimura, K Vandenburgh, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|August 28, 2001
Analysis of speech characteristics in children with velocardiofacial syndrome (VCFS) and children with phenotypic overlap without VCFSL L D'Antonio, N J Scherer, L L Miller, et al.
Pageof 2