M. Berry

发表

Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome

M. Keshavan, V. Shashi, T. Howard, 2010, Psychiatry Research: Neuroimaging.

Vasomotor instability in neonates with chromosome 22q11 deletion syndrome

V. Shashi, M. Hines, M. Berry, 2003, American journal of medical genetics. Part A.

A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.

V. Shashi, T. Hart, J. Sciote, 2000, American journal of human genetics.

Cantú syndrome: Report of nine new cases and expansion of the clinical phenotype

S. Robertson, D. Goudie, V. Shashi, 2011, American journal of medical genetics. Part A.

Down syndrome due to a recombination of a chromosome 21 paracentric inversion in 1 of 2 cases with a review of paracentric recombinants

P. N. Rao, T. Jewett, M. Berry, 1994 .

Partial duplication of 4q12q13 leads to a mild phenotype.

V. Shashi, M. Pettenati, M. Berry, 1999, American journal of medical genetics.

De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay.

J. Shendure, P. Kaplan, C. Haldeman-Englert, 2015, American journal of human genetics.

Prenatal diagnosis of complete sole trisomy 1q

V. Shashi, M. Harper, M. Pettenati, 2001, Prenatal diagnosis.

Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome

Kathryn E. Lewandowski, Matcheri S. Keshavan, Thomas R. Kwapil, 2004, NeuroImage.

The RBMX gene as a candidate for the Shashi X‐linked intellectual disability syndrome

A. Need, V. Shashi, K. Schoch, 2015, Clinical Genetics.

Prenatal interphase detection by FISH of a sex chromosome mosaicism when cytogenetics reports a pseudomosaicism

P. N. Rao, M. Pettenati, J. Rosnes, 1999, Prenatal Diagnosis.

De novo Mutations in NALCN Cause a Syndrome of Congenital Contractures of the Limbs and Face with Hypotonia, and Developmental Delay

J. Shendure, P. Kaplan, C. Haldeman-Englert, 2015, bioRxiv.

COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome

M. Keshavan, V. Shashi, K. Schoch, 2010, Psychiatry Research.

Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome

M. Keshavan, V. Shashi, T. Kwapil, 2006, Clinical genetics.