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Chong Ae Kim

Showing results (21-30 of 150) with videos related to

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Pro-Fono : Revista De Atualizacao Cientifica|November 25, 2010
Behavioral and cognitive phenotype of children and adolescents with Williams-Beuren SyndromeMaria Cristina Triguero Veloz Teixeira, Camila Rondinelli Cobra Monteiro, Renata de Lima Velloso, et al.
Clinics (Sao Paulo, Brazil)|August 3, 2011
Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markersRoberta Lelis Dutra, Patrícia de Campos Pieri, Ana Carolina Dias Teixeira, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|October 29, 2009
Dental evaluation of Kabuki syndrome patientsCamila Santos Teixeira, Claudia Renata Leite Silva, Rachel Sayuri Honjo, et al.
Genes|February 27, 2026
Adaptive and Behavioral Phenotype in Pediatric 22q11.2 Deletion Syndrome: Characterizing a High-Risk Neurogenetic Copy Number VariantLarissa Salustiano Evangelista Pimenta, Claudia Berlim de Mello, Guilherme V Polanczyk, et al.
Clinics (Sao Paulo, Brazil)|November 5, 2010
DiGeorge Syndrome: a not so rare diseaseAngela B F Fomin, Antonio Carlos Pastorino, Chong Ae Kim, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|June 22, 2013
Challenges in the orthodontic treatment of a patient with pycnodysostosisMárcio Vieira Ortegosa, Débora Romeo Bertola, Meire Aguena, et al.
American Journal of Medical Genetics. Part A|April 3, 2016
Nutritional aspects of Noonan syndrome and Noonan-related disordersFernanda Marchetto da Silva, Alexander Augusto Jorge, Alexandra Malaquias, et al.
Clinics (Sao Paulo, Brazil)|June 3, 2009
Nephrogenic diabetes insipidus (NDI): clinical, laboratory and genetic characterization of five Brazilian patientsMaria Helena Vaisbich, Juliana Carneiro, Wolfanga Bóson, et al.
Molecular Biology Reports|March 1, 2022
Frequency of carriers for rare metabolic diseases in a Brazilian cohort of 320 patientsCaio Robledo D' Angioli Costa Quaio, Caroline Monaco Moreira, Christine Hsiaoyun Chung, et al.
Revista Do Hospital Das Clinicas|May 4, 2004
Hydronephrosis in Schinzel-Giedion syndrome: an important clue for the diagnosisLilian Maria José Albano, Paula Priscila Ohara Sakae, Marta Maria Galli Bozzo Mataloun, et al.
Pageof 15

Showing results (21-30 of 150) with videos related to

Sort By:
Pageof 15
Pro-Fono : Revista De Atualizacao Cientifica|November 25, 2010
Behavioral and cognitive phenotype of children and adolescents with Williams-Beuren SyndromeMaria Cristina Triguero Veloz Teixeira, Camila Rondinelli Cobra Monteiro, Renata de Lima Velloso, et al.
Clinics (Sao Paulo, Brazil)|August 3, 2011
Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markersRoberta Lelis Dutra, Patrícia de Campos Pieri, Ana Carolina Dias Teixeira, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|October 29, 2009
Dental evaluation of Kabuki syndrome patientsCamila Santos Teixeira, Claudia Renata Leite Silva, Rachel Sayuri Honjo, et al.
Genes|February 27, 2026
Adaptive and Behavioral Phenotype in Pediatric 22q11.2 Deletion Syndrome: Characterizing a High-Risk Neurogenetic Copy Number VariantLarissa Salustiano Evangelista Pimenta, Claudia Berlim de Mello, Guilherme V Polanczyk, et al.
Clinics (Sao Paulo, Brazil)|November 5, 2010
DiGeorge Syndrome: a not so rare diseaseAngela B F Fomin, Antonio Carlos Pastorino, Chong Ae Kim, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|June 22, 2013
Challenges in the orthodontic treatment of a patient with pycnodysostosisMárcio Vieira Ortegosa, Débora Romeo Bertola, Meire Aguena, et al.
American Journal of Medical Genetics. Part A|April 3, 2016
Nutritional aspects of Noonan syndrome and Noonan-related disordersFernanda Marchetto da Silva, Alexander Augusto Jorge, Alexandra Malaquias, et al.
Clinics (Sao Paulo, Brazil)|June 3, 2009
Nephrogenic diabetes insipidus (NDI): clinical, laboratory and genetic characterization of five Brazilian patientsMaria Helena Vaisbich, Juliana Carneiro, Wolfanga Bóson, et al.
Molecular Biology Reports|March 1, 2022
Frequency of carriers for rare metabolic diseases in a Brazilian cohort of 320 patientsCaio Robledo D' Angioli Costa Quaio, Caroline Monaco Moreira, Christine Hsiaoyun Chung, et al.
Revista Do Hospital Das Clinicas|May 4, 2004
Hydronephrosis in Schinzel-Giedion syndrome: an important clue for the diagnosisLilian Maria José Albano, Paula Priscila Ohara Sakae, Marta Maria Galli Bozzo Mataloun, et al.
Pageof 15