Works matching AU Sathanoori, Malini

Results: 9

Three Supernumerary Marker Chromosomes in a Patient with Developmental Delay,Mental Retardation, and Dysmorphic Features.

Published in:

Genetics Research International, 2011, p. 1, doi. 10.4061/2011/185271

By:

Jie Hu;
Madan-Khetarpal, Suneeta;
Russi, Alvaro H. Serrano;
Kochmar, Sally;
DeWard, Stephanie J.;
Sathanoori, Malini;
Surti, Urvashi

Publication type:

Article

CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders.

Published in:

Journal of Neurodevelopmental Disorders, 2015, v. 7, n. 1, p. 1, doi. 10.1186/s11689-015-9122-9

By:

Hu, Jie;
Liao, Jun;
Sathanoori, Malini;
Kochmar, Sally;
Sebastian, Jessica;
Yatsenko, Svetlana;
Surti, Urvashi

Publication type:

Article

Prenatal Diagnosis of 2q32 Deletion Syndrome Characterized by Multiple Segmental Deletions and Complex Chromosomal Rearrangement Involving Chromosomes 2, 5 and 7.

Published in:

Fetal Diagnosis & Therapy, 2012, v. 31, n. 3, p. 196, doi. 10.1159/000335650

By:

Thorson, Heidi L.;
Surti, Urvashi;
Sathanoori, Malini;
Kochmar, Sally J.;
Torchia, Beth;
Rajkovic, Aleksandar

Publication type:

Article

Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype.

Published in:

Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1166, doi. 10.1002/pd.3977

By:

Liao, Jun;
Sathanoori, Malini;
Yatsenko, Svetlana A.;
Hu, Jie;
Kochmar, Sally J.;
Hoffner, Lori;
Hogge, W. Allen;
Surti, Urvashi

Publication type:

Article

A novel maternally inherited 8q24.3 and a rare paternally inherited 14q23.3 CNVs in a family with neurodevelopmental disorders.

Published in:

American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 8, p. 1921, doi. 10.1002/ajmg.a.37110

By:

Hu, Jie;
Sathanoori, Malini;
Kochmar, Sally;
Azage, Meron;
Mann, Susan;
Madan‐Khetarpal, Suneeta;
Goldstein, Amy;
Surti, Urvashi

Publication type:

Article

Co-existence of 9p deletion and Silver-Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11.

Published in:

American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 1, p. 179, doi. 10.1002/ajmg.a.35658

By:

Hu, Jie;
Sathanoori, Malini;
Kochmar, Sally;
Madan‐Khetarpal, Suneeta;
McGuire, Marianne;
Surti, Urvashi

Publication type:

Article

Whole-Genome Single Nucleotide Polymorphism Array Analysis Is Complementary to Classical Cytogenetic Analysis in the Evaluation of Lymphoid Proliferations.

Published in:

American Journal of Clinical Pathology, 2014, v. 141, n. 2, p. 247, doi. 10.1309/AJCPRHGHT28DUWLA

By:

Gibson, Sarah E.;
Jianhua Luo;
Sathanoori, Malini;
Jun Liao;
Surti, Urvashi;
Swerdlow, Steven H.

Publication type:

Article

Cytogenetic Abnormalities Detected by Fluorescence In Situ Hybridization on Paraffin-Embedded Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Lymphoid Tissue Biopsy Specimens.

Published in:

American Journal of Clinical Pathology, 2008, v. 130, n. 4, p. 620, doi. 10.1309/H9AREV6E2JTMEC6J

By:

Melina Flanagan;
Malini Sathanoori;
Urvashi Surti;
Lorinda Soma;
Steven Swerdlow

Publication type:

Article

Deletion of conserved non‐coding sequences downstream from NKX2‐1: A novel disease‐causing mechanism for benign hereditary chorea.

Published in:

Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 4, p. 1, doi. 10.1002/mgg3.1647

By:

Liao, Jun;
Coffman, Keith A.;
Locker, Joseph;
Padiath, Quasar S.;
Nmezi, Bruce;
Filipink, Robyn A.;
Hu, Jie;
Sathanoori, Malini;
Madan‐Khetarpal, Suneeta;
McGuire, Marianne;
Schreiber, Allison;
Moran, Rocio;
Friedman, Neil;
Hoffner, Lori;
Rajkovic, Aleksandar;
Yatsenko, Svetlana A.;
Surti, Urvashi

Publication type:

Article