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Molecular and Cellular Endocrinology
|
May 26, 2006
Circadian rhythm disorder in a rare disease: Smith-Magenis syndrome
Hélène De Leersnyder, Bruno Claustrat, Arnold Munnich, et al.
European Journal of Medical Genetics
|
May 24, 2008
The genetic basis of inherited anomalies of the teeth. Part 1: clinical and molecular aspects of non-syndromic dental disorders
Isabelle Bailleul-Forestier, Muriel Molla, Alain Verloes, et al.
Clinical Dysmorphology
|
September 15, 2004
Hypertrichosis, Fallot tetralogy, growth and developmental delay
Alain Verloes, Martial Massin, Anne-Catherine Fransolet, et al.
American Journal of Medical Genetics. Part A
|
July 29, 2003
Severely delayed epiphyseal ossification dysplasia with normal stature
Clarisse Baumann, Catherine Garel, Lucille Vuillemain, et al.
American Journal of Medical Genetics. Part A
|
July 20, 2012
Pseudoaminopterin syndrome
Lilia Kraoua, Yline Capri, Laurence Perrin, et al.
Developmental Neuroscience
|
March 18, 2019
Golgipathies in Neurodevelopment: A New View of Old Defects
Sowmyalakshmi Rasika, Sandrine Passemard, Alain Verloes, et al.
American Journal of Medical Genetics
|
November 29, 2002
Spondylometaphyseal dysplasia, east-African type: a new form of early, severe SMD with rounded vertebrae
Alain Verloes, Philippe Lepage, Clarisse Baumann, et al.
American Journal of Medical Genetics. Part A
|
August 9, 2005
Gracile bones, periostal appositions, hypomineralization of the cranial vault, and mental retardation in brothers: milder variant of osteocraniostenosis or new syndrome?
Alain Verloes, Catherine Garel, Stephen Robertson, et al.
European Journal of Human Genetics : EJHG
|
January 13, 2011
Clinical utility gene card for: WAGR syndrome
Carol Clericuzio, Melanie Hingorani, John A Crolla, et al.
American Journal of Medical Genetics. Part A
|
July 21, 2004
New autosomal recessive syndrome with short stature and facio-auriculo-thoracic malformations
André Mégarbané, Linda Daou, Hala Mégarbané, et al.
Page
of 29
Search research articles
Search
Showing results (11-20 of 288) with videos related to
Sort By:
Page
of 29
Molecular and Cellular Endocrinology
|
May 26, 2006
Circadian rhythm disorder in a rare disease: Smith-Magenis syndrome
Hélène De Leersnyder, Bruno Claustrat, Arnold Munnich, et al.
European Journal of Medical Genetics
|
May 24, 2008
The genetic basis of inherited anomalies of the teeth. Part 1: clinical and molecular aspects of non-syndromic dental disorders
Isabelle Bailleul-Forestier, Muriel Molla, Alain Verloes, et al.
Clinical Dysmorphology
|
September 15, 2004
Hypertrichosis, Fallot tetralogy, growth and developmental delay
Alain Verloes, Martial Massin, Anne-Catherine Fransolet, et al.
American Journal of Medical Genetics. Part A
|
July 29, 2003
Severely delayed epiphyseal ossification dysplasia with normal stature
Clarisse Baumann, Catherine Garel, Lucille Vuillemain, et al.
American Journal of Medical Genetics. Part A
|
July 20, 2012
Pseudoaminopterin syndrome
Lilia Kraoua, Yline Capri, Laurence Perrin, et al.
Developmental Neuroscience
|
March 18, 2019
Golgipathies in Neurodevelopment: A New View of Old Defects
Sowmyalakshmi Rasika, Sandrine Passemard, Alain Verloes, et al.
American Journal of Medical Genetics
|
November 29, 2002
Spondylometaphyseal dysplasia, east-African type: a new form of early, severe SMD with rounded vertebrae
Alain Verloes, Philippe Lepage, Clarisse Baumann, et al.
American Journal of Medical Genetics. Part A
|
August 9, 2005
Gracile bones, periostal appositions, hypomineralization of the cranial vault, and mental retardation in brothers: milder variant of osteocraniostenosis or new syndrome?
Alain Verloes, Catherine Garel, Stephen Robertson, et al.
European Journal of Human Genetics : EJHG
|
January 13, 2011
Clinical utility gene card for: WAGR syndrome
Carol Clericuzio, Melanie Hingorani, John A Crolla, et al.
American Journal of Medical Genetics. Part A
|
July 21, 2004
New autosomal recessive syndrome with short stature and facio-auriculo-thoracic malformations
André Mégarbané, Linda Daou, Hala Mégarbané, et al.
Page
of 29