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John M Graham

Showing results (121-130 of 208) with videos related to

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Journal of Pregnancy|April 20, 2016
Pregnancy and Birth Outcomes among Women with Idiopathic Thrombocytopenic PurpuraDiego F Wyszynski, Wendy J Carman, Alan B Cantor, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Molecular and neuroimaging findings in pontocerebellar hypoplasia type 2 (PCH2): is prenatal diagnosis possible?John M Graham, Andrew H Spencer, Inessa Grinberg, et al.
European Journal of Radiology|May 21, 2011
Ovarian cysts on prenatal MRIUrsula Nemec, Stefan F Nemec, Dieter Bettelheim, et al.
American Journal of Human Genetics|April 3, 2012
Exome sequencing identifies PDE4D mutations in acrodysostosisHane Lee, John M Graham, David L Rimoin, et al.
Human Mutation|December 2, 2010
High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndromeTracy Busse, John M Graham, Gerald Feldman, et al.
Prenatal Diagnosis|June 9, 2012
Clubfeet and associated abnormalities on fetal magnetic resonance imagingUrsula Nemec, Stefan F Nemec, Gregor Kasprian, et al.
Journal of Perinatal Medicine|June 3, 2011
Abnormalities of the penis in utero--hypospadias on fetal MRIStefan F Nemec, Gregor Kasprian, Peter C Brugger, et al.
Human Genome Variation|April 16, 2016
Exome sequencing identifies novel mutations in C5orf42 in patients with Joubert syndrome with oral-facial-digital anomaliesIngrid M Wentzensen, Jennifer J Johnston, Kim Keppler-Noreuil, et al.
American Journal of Medical Genetics. Part A|October 14, 2003
A new X-linked syndrome with agenesis of the corpus callosum, mental retardation, coloboma, micrognathia, and a mutation in the Alpha 4 gene at Xq13John M Graham, Patricia Wheeler, Darci Tackels-Horne, et al.
Prenatal Diagnosis|March 5, 2011
Fetal akinesia and associated abnormalities on prenatal MRIStefan F Nemec, Romana Höftberger, Ursula Nemec, et al.
Pageof 21

Showing results (121-130 of 208) with videos related to

Sort By:
Pageof 21
Journal of Pregnancy|April 20, 2016
Pregnancy and Birth Outcomes among Women with Idiopathic Thrombocytopenic PurpuraDiego F Wyszynski, Wendy J Carman, Alan B Cantor, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Molecular and neuroimaging findings in pontocerebellar hypoplasia type 2 (PCH2): is prenatal diagnosis possible?John M Graham, Andrew H Spencer, Inessa Grinberg, et al.
European Journal of Radiology|May 21, 2011
Ovarian cysts on prenatal MRIUrsula Nemec, Stefan F Nemec, Dieter Bettelheim, et al.
American Journal of Human Genetics|April 3, 2012
Exome sequencing identifies PDE4D mutations in acrodysostosisHane Lee, John M Graham, David L Rimoin, et al.
Human Mutation|December 2, 2010
High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndromeTracy Busse, John M Graham, Gerald Feldman, et al.
Prenatal Diagnosis|June 9, 2012
Clubfeet and associated abnormalities on fetal magnetic resonance imagingUrsula Nemec, Stefan F Nemec, Gregor Kasprian, et al.
Journal of Perinatal Medicine|June 3, 2011
Abnormalities of the penis in utero--hypospadias on fetal MRIStefan F Nemec, Gregor Kasprian, Peter C Brugger, et al.
Human Genome Variation|April 16, 2016
Exome sequencing identifies novel mutations in C5orf42 in patients with Joubert syndrome with oral-facial-digital anomaliesIngrid M Wentzensen, Jennifer J Johnston, Kim Keppler-Noreuil, et al.
American Journal of Medical Genetics. Part A|October 14, 2003
A new X-linked syndrome with agenesis of the corpus callosum, mental retardation, coloboma, micrognathia, and a mutation in the Alpha 4 gene at Xq13John M Graham, Patricia Wheeler, Darci Tackels-Horne, et al.
Prenatal Diagnosis|March 5, 2011
Fetal akinesia and associated abnormalities on prenatal MRIStefan F Nemec, Romana Höftberger, Ursula Nemec, et al.
Pageof 21