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American Journal of Medical Genetics. Part A
|
February 5, 2008
X-linked congenital ataxia: a new locus maps to Xq25-q27.1
Ginevra Zanni, Enrico Bertini, Cecelia Bellcross, et al.
American Journal of Medical Genetics. Part A
|
May 20, 2011
A deletion 13q34/duplication 14q32.2-14q32.33 syndrome diagnosed 50 years after neonatal presentation as infantile hypercalcemia
Philip D Pallister, Adam B Pallister, Sarah South, et al.
American Journal of Medical Genetics. Part A
|
May 8, 2013
Elements of morphology: standard terminology for the external genitalia
Raoul C M Hennekam, Judith E Allanson, Leslie G Biesecker, et al.
American Journal of Medical Genetics. Part A
|
December 15, 2006
Nuchal cystic hygroma in five fetuses from 1819 to 1826 in the Meckel-anatomical collections at the University of Halle, Germany
Luminita Göbbel, Rüdiger Schultka, Rudyard Klunker, et al.
American Journal of Medical Genetics. Part A
|
October 14, 2005
A 72-year-old Danish puzzle resolved--comparative analysis of phenotypes in families with different-sized HOXD13 polyalanine expansions
Klaus W Kjaer, Lars Hansen, Hans Eiberg, et al.
American Journal of Medical Genetics. Part A
|
July 29, 2003
Sirenomelia sequence according to the distance between the first sacral vertebra and the ilia
Klaus W Kjaer, Jean W Keeling, John M Opitz, et al.
American Journal of Medical Genetics
|
July 13, 2002
HOXD13 polyalanine tract expansion in classical synpolydactyly type Vordingborg
Klaus Wilbrandt Kjaer, Jess Hedeboe, Merete Bugge, et al.
American Journal of Medical Genetics
|
September 20, 2002
FG syndrome: linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3]
Sabine Dessay, Marie Pierre Moizard, Jean Louis Gilardi, et al.
Fetal and Pediatric Pathology
|
November 9, 2011
Unilateral sclerocornea and tracheal stenosis: unusual findings in a patient with Goldenhar anomaly
Larissa V Furtado, Angelica R Putnam, David H Viskochil, et al.
American Journal of Medical Genetics. Part A
|
April 2, 2004
Mental retardation, Robin sequence, and brachydactyly: further confirmation of a new syndrome
Fiorella Gurrieri, Gioacchino Scarano, Livia Garavelli, et al.
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of 12
Search research articles
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Showing results (81-90 of 116) with videos related to
Sort By:
Page
of 12
American Journal of Medical Genetics. Part A
|
February 5, 2008
X-linked congenital ataxia: a new locus maps to Xq25-q27.1
Ginevra Zanni, Enrico Bertini, Cecelia Bellcross, et al.
American Journal of Medical Genetics. Part A
|
May 20, 2011
A deletion 13q34/duplication 14q32.2-14q32.33 syndrome diagnosed 50 years after neonatal presentation as infantile hypercalcemia
Philip D Pallister, Adam B Pallister, Sarah South, et al.
American Journal of Medical Genetics. Part A
|
May 8, 2013
Elements of morphology: standard terminology for the external genitalia
Raoul C M Hennekam, Judith E Allanson, Leslie G Biesecker, et al.
American Journal of Medical Genetics. Part A
|
December 15, 2006
Nuchal cystic hygroma in five fetuses from 1819 to 1826 in the Meckel-anatomical collections at the University of Halle, Germany
Luminita Göbbel, Rüdiger Schultka, Rudyard Klunker, et al.
American Journal of Medical Genetics. Part A
|
October 14, 2005
A 72-year-old Danish puzzle resolved--comparative analysis of phenotypes in families with different-sized HOXD13 polyalanine expansions
Klaus W Kjaer, Lars Hansen, Hans Eiberg, et al.
American Journal of Medical Genetics. Part A
|
July 29, 2003
Sirenomelia sequence according to the distance between the first sacral vertebra and the ilia
Klaus W Kjaer, Jean W Keeling, John M Opitz, et al.
American Journal of Medical Genetics
|
July 13, 2002
HOXD13 polyalanine tract expansion in classical synpolydactyly type Vordingborg
Klaus Wilbrandt Kjaer, Jess Hedeboe, Merete Bugge, et al.
American Journal of Medical Genetics
|
September 20, 2002
FG syndrome: linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3]
Sabine Dessay, Marie Pierre Moizard, Jean Louis Gilardi, et al.
Fetal and Pediatric Pathology
|
November 9, 2011
Unilateral sclerocornea and tracheal stenosis: unusual findings in a patient with Goldenhar anomaly
Larissa V Furtado, Angelica R Putnam, David H Viskochil, et al.
American Journal of Medical Genetics. Part A
|
April 2, 2004
Mental retardation, Robin sequence, and brachydactyly: further confirmation of a new syndrome
Fiorella Gurrieri, Gioacchino Scarano, Livia Garavelli, et al.
Page
of 12