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John M Opitz

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Journal of Medical Case Reports|June 22, 2011
Opitz trigonocephaly syndrome presenting with sudden unexplained death in the operating room: a case reportLaura Travan, Vanna Pecile, Mariacristina Fertz, et al.
American Journal of Medical Genetics. Part A|August 2, 2005
Male-to-male transmission in Laurin-Sandrow syndrome and exclusion of RARB and RARGKlaus W Kjaer, Lars Hansen, Hans Eiberg, et al.
Fetal and Pediatric Pathology|March 12, 2011
The FG syndrome from a pathological perspectiveCaterina Neri, Karen Moser, Theodore J Pysher, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|June 30, 2011
Cervical ribs are more prevalent in stillborn fetuses than in live-born infants and are strongly associated with fetal aneuploidyLarissa V Furtado, Harshwardhan M Thaker, Lance K Erickson, et al.
The Journal of Urology|June 19, 2007
Genitourinary anomalies of pediatric FG syndromeJames F Smith, Robert O Wayment, Patrick C Cartwright, et al.
American Journal of Medical Genetics. Part A|July 3, 2003
Fetus-in-fetu form of monozygotic twinning with retroperitoneal teratomaEnid Gilbert-Barness, John M Opitz, Diane Debich-Spicer, et al.
Pediatric Neurosurgery|April 11, 2003
Craniocervical anomalies in Dubowitz syndrome. Three cases and a literature reviewKarin R Swartz, Daniel K Resnick, Bermans J Iskandar, et al.
American Journal of Medical Genetics. Part A|June 29, 2010
Recurrence of achondrogenesis type 2 in sibs: Additional evidence for germline mosaicismJessica M Comstock, Angelica R Putnam, Nikhil Sangle, et al.
Fetal and Pediatric Pathology|March 17, 2005
Probable second fetus with Marles-Chudley syndrome: cardiac calcifications with ulnar deficiency and absent/hypoplastic thumbsDavid A Wada, Juliana Szakacs, Anne M Kennedy, et al.
Clinical Dysmorphology|June 3, 2005
Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndromeElisabetta Tabolacci, Marcella Zollino, Rosetta Lecce, et al.
Pageof 12

Showing results (71-80 of 116) with videos related to

Sort By:
Pageof 12
Journal of Medical Case Reports|June 22, 2011
Opitz trigonocephaly syndrome presenting with sudden unexplained death in the operating room: a case reportLaura Travan, Vanna Pecile, Mariacristina Fertz, et al.
American Journal of Medical Genetics. Part A|August 2, 2005
Male-to-male transmission in Laurin-Sandrow syndrome and exclusion of RARB and RARGKlaus W Kjaer, Lars Hansen, Hans Eiberg, et al.
Fetal and Pediatric Pathology|March 12, 2011
The FG syndrome from a pathological perspectiveCaterina Neri, Karen Moser, Theodore J Pysher, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|June 30, 2011
Cervical ribs are more prevalent in stillborn fetuses than in live-born infants and are strongly associated with fetal aneuploidyLarissa V Furtado, Harshwardhan M Thaker, Lance K Erickson, et al.
The Journal of Urology|June 19, 2007
Genitourinary anomalies of pediatric FG syndromeJames F Smith, Robert O Wayment, Patrick C Cartwright, et al.
American Journal of Medical Genetics. Part A|July 3, 2003
Fetus-in-fetu form of monozygotic twinning with retroperitoneal teratomaEnid Gilbert-Barness, John M Opitz, Diane Debich-Spicer, et al.
Pediatric Neurosurgery|April 11, 2003
Craniocervical anomalies in Dubowitz syndrome. Three cases and a literature reviewKarin R Swartz, Daniel K Resnick, Bermans J Iskandar, et al.
American Journal of Medical Genetics. Part A|June 29, 2010
Recurrence of achondrogenesis type 2 in sibs: Additional evidence for germline mosaicismJessica M Comstock, Angelica R Putnam, Nikhil Sangle, et al.
Fetal and Pediatric Pathology|March 17, 2005
Probable second fetus with Marles-Chudley syndrome: cardiac calcifications with ulnar deficiency and absent/hypoplastic thumbsDavid A Wada, Juliana Szakacs, Anne M Kennedy, et al.
Clinical Dysmorphology|June 3, 2005
Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndromeElisabetta Tabolacci, Marcella Zollino, Rosetta Lecce, et al.
Pageof 12