VACTERL/VATER Association

Por Solomon, Benjamin D
Publicado em 2011

Obstacles and opportunities for the future of genomic medicine

Por Solomon, Benjamin D
Publicado em 2014

Genomic Sequencing and the Impact of Molecular Diagnosis on Patient Care

Por Solomon, Benjamin D.
Publicado no Mol Syndromol (2015)

When to Suspect a Genetic Syndrome

Por SOLOMON, BENJAMIN D., MUENKE, MAXIMILIAN
Publicado em 2012

The Benefits of Whole-Genome Sequencing Now and in the Future

Por Khromykh, Alina, Solomon, Benjamin D.
Publicado no Mol Syndromol (2015)

Antigen specific development of mucosal Foxp3+RORγt+ T cells from regulatory T cell precursors

Por Solomon, Benjamin D., Hsieh, Chyi-Song
Publicado no J Immunol (2016)

Holoprosencephaly: A Guide to Diagnosis and Clinical Management

Por Raam, Manu S, Solomon, Benjamin D, Muenke, Maximilian
Publicado em 2011

The Clinical Content of Preconception Care: Genetics and Genomics

Por SOLOMON, Benjamin D., JACK, Brian, FEERO, W. Gregory
Publicado em 2008

Hearing Loss in Syndromic Craniosynostoses: Introduction and Consideration of Mechanisms

Por Agochukwu, Nneamaka B., Solomon, Benjamin D., Muenke, Maximilian
Publicado em 2014

Impact of genetics on the diagnosis and clinical management of syndromic craniosynostoses

Por Agochukwu, Nneamaka B., Solomon, Benjamin D., Muenke, Maximilian
Publicado em 2012

Analysis of genitourinary anomalies in patients with VACTERL (Vertebral anomalies, Anal atresia, Cardiac malformations, Tracheo-Esophageal fistula, Renal anomalies, Limb abnormalit...

Por Solomon, Benjamin D., Raam, Manu S., Pineda-Alvarez, Daniel E.
Publicado em 2011

T-cell selection and intestinal homeostasis

Por Ai, Teresa L., Solomon, Benjamin D., Hsieh, Chyi-Song
Publicado em 2014

Holoprosencephaly in an 8.5-week triploidy gestation

Por Solomon, Benjamin D., Potocki, Lorraine, Oyer, Calvin E., Muenke, Maximilian
Publicado em 2009

Holoprosencephaly and Craniosynostosis: A Report of Two Siblings and Review of the Literature

Por Raam, Manu S., Solomon, Benjamin D., Shalev, Stavit A., Muenke, Maximilian
Publicado em 2010

The Palatal and Oral Manifestations of Muenke Syndrome (FGFR3 related craniosynostosis)

Por Agochukwu, Nneamaka B., Solomon, Benjamin D., Doherty, Emily S., Muenke, Maximilian
Publicado em 2012

Holoprosencephaly due to Numeric Chromosome Abnormalities

Por Solomon, Benjamin D., Rosenbaum, Kenneth N., Meck, Jeanne M., Muenke, Maximilian
Publicado em 2010

Consideration of VACTERL association in patients with trisomy 21

Por Solomon, Benjamin D., Bous, Sophia M., Bianconi, Simona, Pineda-Alvarez, Daniel
Publicado em 2010

A common genetic network underlies substance use disorders and disruptive or externalizing disorders

Por Arcos-Burgos, Mauricio, Vélez, Jorge I., Solomon, Benjamin D., Muenke, Maximilian
Publicado em 2012

Talocalcaneal Coalition in Muenke Syndrome: Report of a patient, review of the literature in FGFR-related craniosynostoses, and consideration of mechanism

Por Agochukwu, Nneamaka B., Solomon, Benjamin D., Benson, Laurel J., Muenke, Maximilian
Publicado em 2013

Epilepsy in Muenke Syndrome: FGFR3-Related Craniosynostosis

Por Agochukwu, Nneamaka B., Solomon, Benjamin D., Gropman, Andrea L., Muenke, Maximilian
Publicado em 2012