VACTERL/VATER Association

od Solomon, Benjamin D
Izdano 2011

Obstacles and opportunities for the future of genomic medicine

od Solomon, Benjamin D
Izdano 2014

Genomic Sequencing and the Impact of Molecular Diagnosis on Patient Care

od Solomon, Benjamin D.
izdano v Mol Syndromol (2015)

When to Suspect a Genetic Syndrome

od SOLOMON, BENJAMIN D., MUENKE, MAXIMILIAN
Izdano 2012

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

od Khromykh, Alina, Solomon, Benjamin D.
izdano v Mol Syndromol (2015)

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

od Solomon, Benjamin D., Hsieh, Chyi-Song
izdano v J Immunol (2016)

Holoprosencephaly: A Guide to Diagnosis and Clinical Management

od Raam, Manu S, Solomon, Benjamin D, Muenke, Maximilian
Izdano 2011

The Clinical Content of Preconception Care: Genetics and Genomics

od SOLOMON, Benjamin D., JACK, Brian, FEERO, W. Gregory
Izdano 2008

Hearing Loss in Syndromic Craniosynostoses: Introduction and Consideration of Mechanisms

od Agochukwu, Nneamaka B., Solomon, Benjamin D., Muenke, Maximilian
Izdano 2014

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

od Agochukwu, Nneamaka B., Solomon, Benjamin D., Muenke, Maximilian
Izdano 2012

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

od Solomon, Benjamin D., Raam, Manu S., Pineda-Alvarez, Daniel E.
Izdano 2011

T-cell selection and intestinal homeostasis

od Ai, Teresa L., Solomon, Benjamin D., Hsieh, Chyi-Song
Izdano 2014

Holoprosencephaly in an 8.5-week triploidy gestation

od Solomon, Benjamin D., Potocki, Lorraine, Oyer, Calvin E., Muenke, Maximilian
Izdano 2009

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

od Raam, Manu S., Solomon, Benjamin D., Shalev, Stavit A., Muenke, Maximilian
Izdano 2010

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

od Agochukwu, Nneamaka B., Solomon, Benjamin D., Doherty, Emily S., Muenke, Maximilian
Izdano 2012

Holoprosencephaly due to Numeric Chromosome Abnormalities

od Solomon, Benjamin D., Rosenbaum, Kenneth N., Meck, Jeanne M., Muenke, Maximilian
Izdano 2010

Consideration of VACTERL association in patients with trisomy 21

od Solomon, Benjamin D., Bous, Sophia M., Bianconi, Simona, Pineda-Alvarez, Daniel
Izdano 2010

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

od Arcos-Burgos, Mauricio, Vélez, Jorge I., Solomon, Benjamin D., Muenke, Maximilian
Izdano 2012

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

od Agochukwu, Nneamaka B., Solomon, Benjamin D., Benson, Laurel J., Muenke, Maximilian
Izdano 2013

Epilepsy in Muenke Syndrome: FGFR3-Related Craniosynostosis

od Agochukwu, Nneamaka B., Solomon, Benjamin D., Gropman, Andrea L., Muenke, Maximilian
Izdano 2012