Germán Rodríguez Criado - JoVE Visualize

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American Journal of Medical Genetics. Part A|August 25, 2004

Infantile systemic hyalinosis: a clinicopathological studyGermán Rodríguez Criado, Antonio González-Meneses, Manuela Cañadas, et al.

American Journal of Medical Genetics. Part A|May 13, 2005

Higher frequency of uncommon 1.5-2 Mb deletions found in familial cases of 22q11.2 deletion syndromeLuis Fernández, Pablo Lapunzina, Isidora López Pajares, et al.

American Journal of Medical Genetics. Part A|September 15, 2005

Clinical and molecular studies on two further families with Simpson-Golabi-Behmel syndromeGermán Rodríguez-Criado, Luis Magano, Mabel Segovia, et al.

Biology of Sex Differences|February 22, 2018

X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cellsBianca Ho, Keelin Greenlaw, Abeer Al Tuwaijri, et al.

Molecular Psychiatry|May 6, 2018

Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorderSuzanna G M Frints, Aysegul Ozanturk, Germán Rodríguez Criado, et al.

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Showing results (1-10 of 5) with videos related to

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American Journal of Medical Genetics. Part A|August 25, 2004

Infantile systemic hyalinosis: a clinicopathological studyGermán Rodríguez Criado, Antonio González-Meneses, Manuela Cañadas, et al.

American Journal of Medical Genetics. Part A|May 13, 2005

Higher frequency of uncommon 1.5-2 Mb deletions found in familial cases of 22q11.2 deletion syndromeLuis Fernández, Pablo Lapunzina, Isidora López Pajares, et al.

American Journal of Medical Genetics. Part A|September 15, 2005

Clinical and molecular studies on two further families with Simpson-Golabi-Behmel syndromeGermán Rodríguez-Criado, Luis Magano, Mabel Segovia, et al.

Biology of Sex Differences|February 22, 2018

X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cellsBianca Ho, Keelin Greenlaw, Abeer Al Tuwaijri, et al.

Molecular Psychiatry|May 6, 2018

Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorderSuzanna G M Frints, Aysegul Ozanturk, Germán Rodríguez Criado, et al.

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