Ankita Patel

P. Stankiewicz, Z. Xia, Ankita Patel, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Accurate description of DNA-based noninvasive prenatal screening.

Ankita Patel, S. Cheung, T. Leung, 2015, The New England journal of medicine.

Adult Low-Hypodiploid Acute B-Lymphoblastic Leukemia With IKZF3 Deletion and TP53 Mutation: Comparison With Pediatric Patients.

Ankita Patel, F. Appelbaum, K. Eaton, 2015, American journal of clinical pathology.

Expanding the genotype–phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysis

P. Stankiewicz, Ankita Patel, S. Cheung, 2013, American journal of medical genetics. Part A.

Parental somatic mosaicism is underrecognized and influences recurrence risk of genomic disorders.

L. Vissers, R. Pfundt, P. Stankiewicz, 2014, American journal of human genetics.

Universal Prenatal Chromosomal Microarray Analysis: Additive Value and Clinical Dilemmas in Fetuses with a Normal Karyotype

Ankita Patel, S. Cheung, A. Beaudet, 2016, American Journal of Perinatology.

Characterization of the human gene encoding alpha-aminoadipate aminotransferase (AADAT).

Ankita Patel, M. Geraghty, C. Jakobs, 2002, Molecular Genetics and Metabolism.

Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43–q44

P. Stankiewicz, Ankita Patel, S. Cheung, 2011, European Journal of Human Genetics.

Rescue karyotyping: a case series of array-based comparative genomic hybridization evaluation of archival conceptual tissue

Marilyn M. Li, Ankita Patel, Z. Williams, 2014, Reproductive Biology and Endocrinology.

Human subtelomeric copy number gains suggest a DNA replication mechanism for formation: beyond breakage–fusion–bridge for telomere stabilization

Ankita Patel, J. Lupski, S. Cheung, 2012, Human Genetics.

11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesity

Ankita Patel, Marwan Shinawi, Ankita Patel, 2011, American journal of medical genetics. Part A.

Comprehensive 5-year study of cytogenetic aberrations in 668 infertile men.

Ankita Patel, S. Cheung, M. Matzuk, 2010, The Journal of urology.

Tetrasomy 13q mosaicism associated with phylloid hypomelanosis and precocious puberty

Ankita Patel, F. Scaglia, S. Dhar, 2009, American journal of medical genetics. Part A.

Chromosomal microarray versus karyotyping for prenatal diagnosis.

D. Ledbetter, L. Shaffer, Ankita Patel, 2012, The New England journal of medicine.

The Xp contiguous deletion syndrome and autism

Ankita Patel, M. Shinawi, F. Scaglia, 2009, American journal of medical genetics. Part A.

Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: A study of 5,380 cases

P. Stankiewicz, L. Shao, Ankita Patel, 2008, American journal of medical genetics. Part A.

Array comparative genomic hybridization detects chromosomal abnormalities in hematological cancers that are not detected by conventional cytogenetics.

L. Shao, Ankita Patel, C. Shaw, 2010, The Journal of molecular diagnostics : JMD.

Clinical Implementation of Chromosomal Microarray Analysis: Summary of 2513 Postnatal Cases

Z. Ou, P. Stankiewicz, M. L. Cooper, 2007, PloS one.

Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders

P. Stankiewicz, Ankita Patel, S. Cheung, 2012, European Journal of Human Genetics.

Validation of a targeted DNA microarray for the clinical evaluation of recurrent abnormalities in chronic lymphocytic leukemia

A. C. Chinault, Ankita Patel, C. Shaw, 2008, American journal of hematology.

Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

J. Rosenfeld, P. Stankiewicz, P. Szafranski, 2017, Human Genetics.

Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region

K. Gunderson, Ankita Patel, J. Lupski, 2007, Genetics in Medicine.

A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes

P. Stankiewicz, Z. Xia, Ankita Patel, 2009, Nature Genetics.

22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome.

Jonathan Berg, Ankita Patel, Z. Ou, 2008, American journal of human genetics.

An Organismal CNV Mutator Phenotype Restricted to Early Human Development

Klaudia Walter, M. Hurles, P. Stankiewicz, 2017, Cell.

Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testing

P. Stankiewicz, J. Wiszniewska, Ankita Patel, 2013, European Journal of Human Genetics.

Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males

Ankita Patel, J. Lupski, S. Cheung, 2006, Genetics in Medicine.

Phenotypic manifestations of copy number variation in chromosome 16p13.11

P. Stankiewicz, E. Roeder, Ankita Patel, 2011, European Journal of Human Genetics.

Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes

Z. Ou, E. Roeder, V. Enciso, 2008, Genetics in Medicine.

Genomic Imbalances in Neonates With Birth Defects: High Detection Rates by Using Chromosomal Microarray Analysis

P. Stankiewicz, P. Stankiewicz, Ankita Patel, 2008, Pediatrics.

OEIS complex associated with chromosome 1p36 deletion: A case report and review

A. Breman, Ankita Patel, S. Cheung, 2010, American journal of medical genetics. Part A.

Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?

P. Stankiewicz, Z. Xia, J. Wiszniewska, 2010, Human mutation.

Co-occurrence of recurrent duplications of the DiGeorge syndrome region on both chromosome 22 homologues due to inherited and de novo events

P. Stankiewicz, J. Wiszniewska, Ankita Patel, 2012, Journal of Medical Genetics.

Duplication of chromosome band 12q24.11q24.23 results in apparent Noonan syndrome

J. Wiszniewska, A. C. Chinault, Ankita Patel, 2008, American journal of medical genetics. Part A.

Parental somatic mosaicism for CNV deletions - A need for more sensitive and precise detection methods in clinical diagnostics settings.

Justyna A. Karolak, J. Rosenfeld, P. Stankiewicz, 2020, Genomics.

Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases

P. Stankiewicz, A. Breman, Ankita Patel, 2019, Genome Medicine.

Mechanisms for Complex Chromosomal Insertions

P. Stankiewicz, A. Breman, P. Szafranski, 2016, PLoS genetics.

Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3.

P. Stankiewicz, Ankita Patel, C. Shaw, 2015, Human molecular genetics.

Human endogenous retroviral elements promote genome instability via non-allelic homologous recombination

J. Rosenfeld, P. Stankiewicz, Ankita Patel, 2014, BMC Biology.

Recurrent HERV‐H‐Mediated 3q13.2–q13.31 Deletions Cause a Syndrome of Hypotonia and Motor, Language, and Cognitive Delays

J. Rosenfeld, L. Shaffer, P. Stankiewicz, 2013, Human mutation.

NAHR-mediated copy-number variants in a clinical population: Mechanistic insights into both genomic disorders and Mendelizing traits

J. Rosenfeld, P. Stankiewicz, A. Breman, 2013, Genome research.

Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplications.

P. Stankiewicz, J. Wiszniewska, M. L. Cooper, 2011, Human molecular genetics.

Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching.

P. Stankiewicz, Ankita Patel, C. Shaw, 2009, Human molecular genetics.

Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

Tomas W. Fitzgerald, D. J. Driscoll, N. Carter, 2009, American journal of human genetics.

Development and validation of a CGH microarray for clinical cytogenetic diagnosis

Chad A Shaw, Ankita Patel, Z. Ou, 2005, Genetics in Medicine.

Chromosomal Microarray Analysis Using Array Comparative Genomic Hybridization on DNA from Amniotic Fluid and Chorionic Villus Sampling.

Ankita Patel, 2018, Methods in molecular biology.

Identification of novel candidate disease genes from de novo exonic copy number variants

Lisa T. Emrick, J. Rosenfeld, P. Stankiewicz, 2017, Genome Medicine.

Chromosomal Microarrays: Understanding Genetics of Neurodevelopmental Disorders and Congenital Anomalies

J. Rosenfeld, Ankita Patel, 2016, Journal of Pediatric Genetics.

Application of DNA Microarray to Clinical Diagnostics.

Ankita Patel, S. Cheung, 2016, Methods in molecular biology.

Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today’s genomic array era?

P. Stankiewicz, Ankita Patel, C. Shaw, 2012, Genetics in Medicine.

Phenotypic spectrum and genotype–phenotype correlations of NRXN1 exon deletions

P. Stankiewicz, Ankita Patel, S. Cheung, 2012, European Journal of Human Genetics.

Suspected trisomy 22: Modification, clarification, or confirmation of the diagnosis by aCGH

Ankita Patel, S. Cheung, J. Belmont, 2011, American journal of medical genetics. Part A.

Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories

S. Schwartz, L. Shaffer, Ankita Patel, 2009, Genetics in Medicine.

Microarray‐based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics

P. Stankiewicz, Ankita Patel, C. Shaw, 2007, American journal of medical genetics. Part A.

Human subtelomeric copy number gains suggest a DNA replication mechanism for formation: beyond breakage–fusion–bridge for telomere stabilization

Ankita Patel, J. Lupski, S. Cheung, 2012, Human Genetics.

Characterization of chromosomal abnormalities in pregnancy losses reveals critical genes and loci for human early development

P. Stankiewicz, A. Breman, Ankita Patel, 2017, Human mutation.

Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes

Ankita Patel, S. Lalani, D. M. Martin, 2015, American journal of medical genetics. Part A.

ipt Recurrent Deletions and Duplications of Chromosome 2 q 11 . 2 and 2 q 13 are Associated with Variable Outcomes

Donna M. Martin, Ankita Patel, S. Lalani, 2015 .

Molecular findings among patients referred for clinical whole-exome sequencing: Editorial comment

Ankita Patel, J. Lupski, R. Gibbs, 2015 .

Haploinsufficiency of the LIM domain containing preferred translocation partner in lipoma (LPP) gene in patients with tetralogy of Fallot and VACTERL association

Ankita Patel, N. Bowles, Cammon B. Arrington, 2010, American journal of medical genetics. Part A.

Low‐level mosaicism of trisomy 14: Phenotypic and molecular characterization

L. Shao, Ankita Patel, C. Shaw, 2008, American journal of medical genetics. Part A.

Prenatal diagnosis of a 9q34.3 microdeletion by array‐CGH in a fetus with an apparently balanced translocation

Ankita Patel, J. Lupski, S. Cheung, 2007, Prenatal diagnosis.

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

L. D. White, Ankita Patel, C. Shaw, 2009, Prenatal diagnosis.

Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH

L. D. White, A. Breman, Ankita Patel, 2008, Prenatal diagnosis.

Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses

L. D. White, Z. Ou, A. C. Chinault, 2008, Genetics in Medicine.

Microarray-based comparative genomic hybridization using sex-matched reference DNA provides greater sensitivity for detection of sex chromosome imbalances than array-comparative genomic hybridization with sex-mismatched reference DNA.

Z. Ou, A. C. Chinault, Ankita Patel, 2009, The Journal of molecular diagnostics : JMD.

Clinical Applications of Microarrays in Cancer

Marilyn M. Li, Ankita Patel, Xiaofeng Hu, 2012 .

Somatic mosaicism detected by exon-targeted, high-resolution aCGH in 10 362 consecutive cases

P. Stankiewicz, Ankita Patel, C. Shaw, 2014, European Journal of Human Genetics.

Chromosomal microarray versus karyotyping for prenatal diagnosis

D. Ledbetter, L. Shaffer, Ankita Patel, 2013 .

Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature

A. Breman, Ankita Patel, C. Shaw, 2012, Prenatal diagnosis.

Subtelomeric deletion of chromosome 10p15.3: Clinical findings and molecular cytogenetic characterization

J. Rosenfeld, I. Krantz, N. Spinner, 2012, American journal of medical genetics. Part A.

Triploidy mosaicism (45,X/68,XX) in an infant presenting with failure to thrive

A. Breman, Ankita Patel, J. Posey, 2016, American journal of medical genetics. Part A.

Insertional translocation detected using FISH confirmation of array‐comparative genomic hybridization (aCGH) results

Z. Ou, P. Stankiewicz, M. L. Cooper, 2010, American journal of medical genetics. Part A.

De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder.

Stephan J Sanders, R. Redon, J. Rosenfeld, 2017, American journal of human genetics.

De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder.

Stephan J Sanders, R. Redon, J. Rosenfeld, 2017, American journal of human genetics.

The phenotype of recurrent 10q22q23 deletions and duplications

R. Pfundt, P. Stankiewicz, Ankita Patel, 2011, European Journal of Human Genetics.

Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping

Z. Ou, P. Stankiewicz, Ankita Patel, 2009, Human Genetics.

A genome‐wide screen for copy number alterations in Aicardi syndrome

Ankita Patel, R. Lewis, V. Sutton, 2009, American journal of medical genetics. Part A.

MECP2 duplications in six patients with complex sex chromosome rearrangements

A. Breman, Ankita Patel, S. Cheung, 2011, European Journal of Human Genetics.

Incidental Finding in Copy Number Variation (CNV) Analysis

Ankita Patel, W. Bi, 2014, Current Genetic Medicine Reports.

Fusion of Large-Scale Genomic Knowledge and Frequency Data Computationally Prioritizes Variants in Epilepsy

Ankita Patel, Chad A. Shaw, Carlos A. Bacino, 2013, PLoS genetics.

A case report: Twin pregnancy Patient with Tuberculosis

Ankita Patel, V. Bhola, Jayshree Narshetty, 2014 .

Correction: Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen)

S. South, Ankita Patel, E. Thorland, 2021, Genetics in Medicine.

Incidental copy-number variants identified by routine genome testing in a clinical population

P. Stankiewicz, Ankita Patel, C. Shaw, 2012, Genetics in Medicine.

Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives

Ankita Patel, S. Cheung, P. Ward, 2008, Genetics in Medicine.

SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delay

P. Stankiewicz, Ankita Patel, Yiping Shen, 2013, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

SHANK3 overexpression causes manic-like behavior with unique pharmacogenetic properties

A. Breman, Ankita Patel, S. Cheung, 2013, Nature.

Expanding the clinical spectrum of the 16p11.2 chromosomal rearrangements: three patients with syringomyelia

Ankita Patel, J. Hunter, M. Shinawi, 2011, European Journal of Human Genetics.

Recurrent distal 7q11.23 deletion including HIP1 and YWHAG identified in patients with intellectual disabilities, epilepsy, and neurobehavioral problems.

P. Stankiewicz, Z. Xia, P. Szafranski, 2010, American journal of human genetics.

Cryptic unbalanced translocation t(17;18)(p13.2;q22.3) identified by subtelomeric FISH and defined by array‐based comparative genomic hybridization in a patient with mental retardation and dysmorphic features

Z. Ou, P. Stankiewicz, M. L. Cooper, 2005, American journal of medical genetics. Part A.

Confounding by Repetitive Elements and CpG Islands Does Not Explain the Association between Hypomethylation and Genomic Instability

L. D. White, A. C. Chinault, Ankita Patel, 2013, PLoS genetics.

MCTP2 is a dosage-sensitive gene required for cardiac outflow tract development.

Ankita Patel, S. Cheung, J. Belmont, 2013, Human molecular genetics.

The importance of phase analysis in multiexon copy number variation detected by aCGH in autosomal recessive disorder loci

Ankita Patel, C. Schaaf, M. Gillentine, 2017, American journal of medical genetics. Part A.

Clinical characterization of int22h1/int22h2-mediated Xq28 duplication/deletion: new cases and literature review

E. Roeder, Ankita Patel, S. Cheung, 2015, BMC Medical Genetics.

TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.

Gao T. Wang, Mahshid S. Azamian, M. Hurles, 2013, American journal of human genetics.

Preparation of Chorionic Villus Samples for Metaphase Chromosome Analysis and Chromosomal Microarray Analysis

A. Breman, Ankita Patel, Amy M. Breman, 2012, Current protocols in human genetics.

Mosaic tetrasomy 12p with triplication of 12p detected by array‐based comparative genomic hybridization of peripheral blood DNA

K. Gunderson, M. L. Cooper, Ankita Patel, 2007, American journal of medical genetics. Part A.

Mohr-Claussen Syndrome: A Rare Case.

Ankita Patel, M. Joshi, Namish Batra, 2016, Journal of clinical and diagnostic research : JCDR.

A reciprocal translocation 46,XY,t(8;9)(p11.2;q13) in a bladder exstrophy patient disrupts CNTNAP3 and presents evidence of a pericentromeric duplication on chromosome 9.

S. South, Ankita Patel, G. Stetten, 2005, Genomics.

Clinical and molecular characterization of a patient with Langer–Giedion syndrome and mosaic del(8)(q22.3q24.13)

Ankita Patel, B. Levy, H. Lüdecke, 2008, American Journal of Medical Genetics. Part A.

Response to Maya et al.

S. South, Ankita Patel, E. Thorland, 2020, Genetics in Medicine.

Novel deletion of 6p21.31p21.1 associated with laryngeal cleft, developmental delay, dysmorphic features and vascular anomaly.

A. Breman, Ankita Patel, Dana Marafi, 2019, European journal of medical genetics.

Erratum: De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder (American Journal of Human Genetics (2017) 100(2) (352–363) (S0002929717300034) (10.1016/j.ajhg.2017.01.003))

Stephan J Sanders, R. Redon, J. Rosenfeld, 2017 .

Identification of novel candidate disease genes from de novo exonic copy number variants

J. Rosenfeld, P. Stankiewicz, A. Breman, 2017, Genome Medicine.

Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies

J. Rosenfeld, I. Krantz, Ankita Patel, 2019, Genetics in Medicine.

Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive function

P. Stankiewicz, Ankita Patel, S. Cheung, 2012, neurogenetics.

De novo terminal 22q12.3q13.3 duplication with pituitary hypoplasia

Ankita Patel, R. Rauch, R. Heptulla, 2009, American Journal of Medical Genetics. Part A.

Frequency and pattern of karyotypic abnormalities in human prostate cancer.

Ankita Patel, J. McNeal, D. Peehl, 1990, Cancer research.

Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders

P. Stankiewicz, Ankita Patel, J. Lupski, 2009, Journal of Medical Genetics.

Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies

Rebecca C. Spillmann, Denise L. Perry, J. Rosenfeld, 2019, Genetics in Medicine.

Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases

P. Stankiewicz, Ankita Patel, C. Shaw, 2019, Genome Medicine.

Microdeletions including YWHAE in the Miller–Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment

Z. Ou, P. Stankiewicz, Ankita Patel, 2009, Journal of Medical Genetics.

Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

J. Rosenfeld, P. Stankiewicz, P. Szafranski, 2017, Human Genetics.

Vaccine‐associated varicella and rubella infections in severe combined immunodeficiency with isolated CD4 lymphocytopenia and mutations in IL7R detected by tandem whole exome sequencing and chromosomal microarray

Magalie S Leduc, Ankita Patel, C. Shaw, 2014, Clinical and experimental immunology.

22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome.

Z. Ou, Ankita Patel, J. Lupski, 2008, American Journal of Human Genetics.

Detection of clinically relevant exonic copy‐number changes by array CGH

P. Stankiewicz, Z. Xia, Ankita Patel, 2010, Human mutation.

Genomic duplication resulting in increased copy number of genes encoding the sister chromatid cohesion complex conveys clinical consequences distinct from Cornelia de Lange

A. C. Chinault, Ankita Patel, J. Lupski, 2008, Journal of Medical Genetics.

Genomic hypomethylation in the human germline associates with structural mutability in the human genome

L. D. White, A. C. Chinault, Ankita Patel, 2012 .

Expanding the genotype–phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysis

P. Stankiewicz, Ankita Patel, M. Bull, 2013, American journal of medical genetics. Part A.

A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes

P. Stankiewicz, Z. Xia, Ankita Patel, 2009, Nature Genetics.

A genome‐wide screen for copy number alterations in Aicardi syndrome

Ankita Patel, R. Lewis, V. Sutton, 2009, American journal of medical genetics. Part A.

The Xp contiguous deletion syndrome and autism

Ankita Patel, M. Shinawi, F. Scaglia, 2009, American journal of medical genetics. Part A.

Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly

P. Stankiewicz, Ankita Patel, J. Lupski, 2005, Journal of Medical Genetics.

MCTP2 is a dosage-sensitive gene required for cardiac outflow tract development.

Ankita Patel, S. Cheung, J. Belmont, 2013, Human molecular genetics.

Deletion Syndrome : Clinical and Molecular Analysis Using Array CGH

Z. Ou, P. Stankiewicz, Ankita Patel, 2010 .

Recurrent HERV‐H‐Mediated 3q13.2–q13.31 Deletions Cause a Syndrome of Hypotonia and Motor, Language, and Cognitive Delays

J. Rosenfeld, L. Shaffer, P. Stankiewicz, 2013, Human mutation.

Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: Clinical report and review

K. Gunderson, M. L. Cooper, Ankita Patel, 2007, American journal of medical genetics. Part A.