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S E McCandless

Showing results (1-10 of 16) with videos related to

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American Journal of Medical Genetics|July 24, 1998
Severe oculocerebrocutaneous (Delleman) syndrome: overlap with Goldenhar anomalyS E McCandless, N H Robin
American Journal of Medical Genetics|June 26, 2001
Metachromatic leukodystrophy in the Navajo: fallout of the American-Indian wars of the nineteenth centuryS Holve, D Hu, S E McCandless
The Journal of Urology|July 1, 1991
Urinary tract malformations in identical twinsS E McCandless, D Uehling, A L Friedman
Archives of Pediatrics & Adolescent Medicine|May 30, 1998
Deletion 22q11: a newly recognized cause of behavioral and psychiatric disordersS E McCandless, J A Scott, N H Robin
American Journal of Medical Genetics|February 7, 1998
Disorganization in mice and humans and its relation to sporadic birth defectsN H Robin, N Abbadi, S E McCandless, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP|March 11, 1999
Case studies: psychological test findings for two children with X-linked adrenoleukodystrophyC E Ievers, R T Brown, S E McCandless, et al.
American Journal of Medical Genetics|November 15, 2000
Adult with an interstitial deletion of chromosome 10 [del(10)(q25. 1q25.3)]: overlap with Coffin-Lowry syndromeS E McCandless, S Schwartz, S Morrison, et al.
Genomics|November 23, 2000
Betaine-homocysteine methyltransferase-2: cDNA cloning, gene sequence, physical mapping, and expression of the human and mouse genesL H Chadwick, S E McCandless, G L Silverman, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|September 30, 2010
Diaphragm dysfunction with congenital cytomegalovirus infectionK Izumi, I Hokuto, S Yamaguchi, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
The tandem mass spectrometry newborn screening experience in North Carolina: 1997-2005D M Frazier, D S Millington, S E McCandless, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics|July 24, 1998
Severe oculocerebrocutaneous (Delleman) syndrome: overlap with Goldenhar anomalyS E McCandless, N H Robin
American Journal of Medical Genetics|June 26, 2001
Metachromatic leukodystrophy in the Navajo: fallout of the American-Indian wars of the nineteenth centuryS Holve, D Hu, S E McCandless
The Journal of Urology|July 1, 1991
Urinary tract malformations in identical twinsS E McCandless, D Uehling, A L Friedman
Archives of Pediatrics & Adolescent Medicine|May 30, 1998
Deletion 22q11: a newly recognized cause of behavioral and psychiatric disordersS E McCandless, J A Scott, N H Robin
American Journal of Medical Genetics|February 7, 1998
Disorganization in mice and humans and its relation to sporadic birth defectsN H Robin, N Abbadi, S E McCandless, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP|March 11, 1999
Case studies: psychological test findings for two children with X-linked adrenoleukodystrophyC E Ievers, R T Brown, S E McCandless, et al.
American Journal of Medical Genetics|November 15, 2000
Adult with an interstitial deletion of chromosome 10 [del(10)(q25. 1q25.3)]: overlap with Coffin-Lowry syndromeS E McCandless, S Schwartz, S Morrison, et al.
Genomics|November 23, 2000
Betaine-homocysteine methyltransferase-2: cDNA cloning, gene sequence, physical mapping, and expression of the human and mouse genesL H Chadwick, S E McCandless, G L Silverman, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|September 30, 2010
Diaphragm dysfunction with congenital cytomegalovirus infectionK Izumi, I Hokuto, S Yamaguchi, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
The tandem mass spectrometry newborn screening experience in North Carolina: 1997-2005D M Frazier, D S Millington, S E McCandless, et al.
Pageof 2