Neurocutaneous disease: A practical approach

door Carey, John C.
Gepubliceerd in 1988

Teratogenic Effects of Drugs: A Resource for Clinicians (TERIS)

door Carey, John C.
Gepubliceerd in 1995

The trisomy 18 syndrome

door Cereda, Anna, Carey, John C
Gepubliceerd in 2012

Health-Related Quality of Life Measures in Genetic Disorders: an Outcome Variable for Consideration in Clinical Trials

door Stevenson, David A., Carey, John C.
Gepubliceerd in 2009

New Syndrome: A Novel Multiple Congenital Anomaly-Mental Retardation Syndrome with Pierre Robin Sequence and Cerebellar Hypoplasia in Two Sisters

door Stevenson, David A., Carey, John C.
Gepubliceerd in 2007

Clinical utility gene card for: Wolf–Hirschhorn (4p-) syndrome

door Battaglia, Agatino, South, Sarah, Carey, John C
Gepubliceerd in 2011

Genética médica /

door Jorde, Lynn B., Carey, John C., White, Raymond L.
Gepubliceerd in 1996.

Familial Congenital Nonimmune Hydrops, Chylothorax and Pulmonary Lymphangiectasia

door Stevenson, David A., Pysher, Theodore J., Ward, Robert M., Carey, John C.
Gepubliceerd in 2006

Elements of Morphology: Introduction

door Allanson, Judith E, Biesecker, Leslie G, Carey, John C, Hennekam, Raoul CM
Gepubliceerd in 2009

Clinical and Molecular Aspects of an Informative Family with Neurofibromatosis Type 1 and Noonan Phenotype

door Stevenson, David A., Viskochil, David H., Rope, Alan F., Carey, John C.
Gepubliceerd in 2006

Occurrence and clinical features of epileptic and non-epileptic paroxysmal events in five children with Pallister–Killian syndrome

door Filloux, Francis M., Carey, John C., Krantz, Ian D., Ekstrand, Jeffrey J., Candee, Meghan S.
Gepubliceerd in 2012

Novel de novo ARCN1 intronic variant causes rhizomelic short stature with microretrognathia and developmental delay

door Tidwell, Timothy, Deshotel, Malia, Palumbos, Janice, Miller, Chris, Bayrak-Toydemir, Pinar, Carey, John C.
Gepubliceerd in Cold Spring Harb Mol Case Stud (2020)

Etiology and clinical presentation of birth defects: population based study

door Feldkamp, Marcia L, Carey, John C, Byrne, Janice L B, Krikov, Sergey, Botto, Lorenzo D
Gepubliceerd in BMJ (2017)

Mutations in TNNT3 Cause Multiple Congenital Contractures: A Second Locus for Distal Arthrogryposis Type 2B

door Sung, Sandy S., Brassington, Anna-Marie E., Krakowiak, Patrycja A., Carey, John C., Jorde, Lynn B., Bamshad, Michael
Gepubliceerd in 2003

Plasma Zinc Concentrations of Mothers and the Risk of Oral Clefts in their Children in Utah

door Munger, Ronald G., Tamura, Tsunenobu, Johnston, Kelley E., Feldkamp, Marcia, Pfister, Roxane, Botto, Lorenzo, Carey, John C
Gepubliceerd in 2009

Deletions involving genes WHSC1 and LETM1 may be necessary, but are not sufficient to cause Wolf–Hirschhorn Syndrome

door Andersen, Erica F, Carey, John C, Earl, Dawn L, Corzo, Deyanira, Suttie, Michael, Hammond, Peter, South, Sarah T
Gepubliceerd in 2014

Congenital Chylous Ascites and Ehlers-Danlos Syndrome Type VI

door Ermarth, Anna K., Pohl, John, Esty, Brittany, Sempler, Jessica K., Carey, John C., O’Gorman, Molly A.
Gepubliceerd in ACG Case Rep J (2016)

Motor Proficiency in Children with Neurofibromatosis Type 1

door Johnson, Barbara, MacWilliams, Bruce, Carey, John C., Viskochil, David H., D’Astous, Jacques L., Stevenson, David A.
Gepubliceerd in 2010

Lower Extremity Strength and Hopping and Jumping Ground Reaction forces in Children with Neurofibromatosis Type 1

door Johnson, Barbara, MacWilliams, Bruce, Carey, John C., Viskochil, David H., D’Astous, Jacques L., Stevenson, David A.
Gepubliceerd in 2011

Elements of Morphology: Standard Terminology for the External Genitalia

door Hennekam, Raoul C.M., Allanson, Judith E., Biesecker, Leslie G., Carey, John C., Opitz, John M., Vilain, Eric
Gepubliceerd in Am J Med Genet A (2013)