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Vijaya kumar Pidugu and Usha R Dutta (2012): Fluorescence in .situ Hybridization: Technology and its application in Molecular Medicine. Journal of Cytology and Genetics, 13, 1-8.
Usha R Dutta, Vijaya Kumar Pidugu, Ch Venkateshwar Goud, Christiane Hoefers, Monika Hagemann and Ashwin Dalal (2013). Identification and Molecular Cytogenetic Characterization of a novel complex Y chromosome rearrangement in a boy with disorder of sexual development. GENE 519; 374-380.
Usha R Dutta, Vijaya kumar P, Ashwin B Dalal. (2012): Molecular and Cytogenetic Characterization of Two Patients with Recurrent miscarriages and X-Autosome Translocation. Journal of Research in Medical Sciences 17; 572-4.
Vineeth VS, Suttur S Malini, Sreenivasa G, Usha R Dutta.(2012): High incidence of sperm dysfunction in a varicocele infertile man: case report. Asia Pacific Journal of Reproduction. vol (1), Number 1, March; 61- 64.
A Radha Rama Devi, Usha R Dutta. (2012): Ring chromosome 20 associated with refractory epilepsy: case report. Asian Journal of Medical Sciences 2(2011) 141-144.
Bashyam MD, Chaudhary AK, Manjari S, Nagarajaram HA, Devi AR, Bashyam L, Reddy EC, Dalal A. Molecular genetic analysis of MSUD from India reveals mutations causing altered protein truncation affecting the C-termini of E1α and E1β. J Cell Biochem. 2012 May 16.
Patil SJ, Bhat V, Dalal A, Santosh JS. Confirmation of the Zechi-Ceide syndrome. Am J Med Genet A. 2012;158A(6):1467-71
Angalena R, Aggarwal S, Phadke SR, Dalal A. Compound heterozygote condition in beta thalassemia major due to a novel single nucleotide deletion (-T) at codon 69 in association with IVS 1-5 (G>C) mutation. Int J Lab Hematol. 2012 Mar 12 [Epub ahead of print].
Ponnala R, Ranganath P, Dutta UR, Pidugu VK, Dalal AB. Phenotypic and molecular characterization of partial trisomy 2q resulting from insertion-duplication in chromosome 18q: a case report and review of literature. Cytogenet Genome Res. 2012;136(3):229-34.
Usha R. Dutta , Vijaya Kumar Pidugu, Venkatesh Goud, Ashwin B. Dalal Mosaic Down syndrome with a marker: Molecular cytogenetic characterization of the marker chromosome. Gene. 2011 Dec 28. [Epub ahead of print] PMID:22245181 http://www.ncbi.nlm.nih.gov/pubmed/22245181
Suttur S, Malini, Vijaya Kumar Pidugu, Ashwin B. Dalal, Usha R Dutta. Evaluation of sex chromosomal anomalies in sperms among infertile males by Fluorescence in situ Hybridization. Journal of Cytology & Genetics, vol 12 (NS) 77-84(2011)
Patil SJ, Ponnala R, Shah S, Dalal A.Mosaic Trisomy 9 Presenting with Congenital Heart Disease, Facial Dysmorphism and Pigmentary Skin Lesions: Intricate Issues of Genetic Counseling. Indian J Pediatr. 2011 Oct 6. [Epub ahead of print]
Ponnala R, Dalal A. Partial monosomy 7q. Indian Pediatr. 2011 May 7;48(5):399-401.
Padma Priya T, Dalal AB. Tuberous Sclerosis: Diagnosis and Prenatal Diagnosis by MLPA. Indian J Pediatr. 2011 May 4. [Epub ahead of print]
Kumar R, Panigrahi I, Dalal A, Agarwal S. Sickle Cell Anemia-Molecular Diagnosis and Prenatal Counseling: SGPGI Experience. Indian J Pediatr. 2011 Jun 29. [Epub ahead of print].
M D Bashyam, A K Chaudhary, E C Reddy, V Reddy, V Acharya, H A Nagarajaram, A R R Devi, L Bashyam, A B Dalal, N Gupta, M Kabra, M Agarwal, S R Phadke, R Tainwala, R Kumar, S V Hariharan (2011). An Ectodysplasin A receptor (EDAR) founder mutation results in a high frequency of the autosomal recessive form of Hypohidrotic Ectodermal Dysplasia in India. Br J Dermatol (In Press).
Usha R Dutta, Rajitha P, Vijaya kumar P, Ashwin B Dalal. (2011): Cytogenetic abnormalities in 1162 couples with recurrent miscarriages in southern region of India: report and review. Journal of Assisted Reproduction and Genetics (2) 28: 145- 148. (http://www.ncbi.nlm.nih.gov/pubmed/20931274)
Angalena R, Prabitha KN, Chaudhary AK, Bashyam MD, Jain S, Dalal AB. A novel homozygous point mutation at codon 82 (HBB:c.247A > T)) in the beta-globin gene leads to thalassemia major. Int J Lab Hematol. 2010 Oct;32(5):548-549 (http://www.ncbi.nlm.nih.gov/pubmed/20136848)
Usha R Dutta, Rajitha P, Vijaya kumar P, Ashwin B Dalal. (2011): Molecular Cytogenetics Illustrated: SKY and FISH Usha R Dutta, Vijaya Kumar Pidugu, Ashwin B Dalal, Newsletter of Genetics Chapter of Indian Academy of Pediatrics, Vol 4, Issue 1 (Jan-Mar 2011).
Järn Rüssel, Usha Dutta, Dorothea Wand, Dietmar Schlote, Ingo Hansmann. (2009): The 9p24.3 breakpoint of a constitutional t(6;9)(p12;p24) presenting in a patient with chronic lymphocytic leukemia maps close to the putative promoter region of DMRT2 gene. Cytogenetic and Genome Research 125:81-86.
Dalal AB, Sarkar A, Priya TP, Nandineni MR. Giuffr-Tsukahara syndrome: Evidence for X-linked dominant inheritance and review. Am J Med Genet A. 2010;152A(8):2057-60.(http://www.ncbi.nlm.nih.gov/pubmed/20635354)
Priya TP, Philip N, Molho-Pessach V, Busa T, Dalal A, Zlotogorski A. H syndrome: novel and recurrent mutations in SLC29A3. Br J Dermatol. 2010;162(5):1132-4. (http://www.ncbi.nlm.nih.gov/pubmed/20199539)
Agarwal S, Tamhankar PM, Kumar R, Dalal A. Clinical and haematological features in a compound heterozygote (HBB:c.92 + 5G > C/HBB:c.93-2A > C) case of thalassaemia major. Int J Lab Hematol. 2010;32(3):369-72. (http://onlinelibrary.wiley.com/doi/10.1111/j.1751-553X.2009.01157.x/abstract)
Girisha KM, Vahab SA, Dalal AB, Gopinath PM, Satyamoorthy K. Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis. Ann Hematol. 2010;89(6):625-6. (http://www.ncbi.nlm.nih.gov/pubmed/19727721)
Padma Priya T, Ashwin Dalal. Triplet Primed PCR (TP-PCR) A Versatile Method For Molecular Diagnosis Of Triplet Repeat Disorders. Newsletter of Genetics Chapter of Indian Academy of Pediatrics, Vol 3, Issue 3 (July-Sept 2010)
Kumar R, Tamhankar PM, Panigrahi I, Dalal A, Agarwal S. A novel beta-globin mutation (HBB:c.107A>G; or codon 35 beta (A-->G)) at alpha-beta chain interfaces. Ann Hematol. 2009 ;88(12):1269-71. (http://www.ncbi.nlm.nih.gov/pubmed/19488752)
Ashwin Dalal. Stem cell therapy:Current status. Newsletter of Genetics Chapter of Indian Academy of Pediatrics, Vol 2, Issue 2 (Apr-Jun 2009)
Vinukonda Govindaiah, Shaik Mohammad Naushad, Krishnamurthy Prabhakara, Prasad Chintakindi Krishna, Akella Radha Rama Devi. Association of parental hyperhomocysteinemia and C677T Methylenetetrahydrofolate reductase (MTHFR) polymorphism with recurrent pregnancy loss. Clinical Biochemistry 42 (2009) 380-386
Govindaiah Vinukonda, Naushad Shaik Mohammad, Jamal Md Nurul Jain, Krishna Prasad Chintakindi, Radha Rama Devi Akella. Genetic and environmental influences on total plasma homocysteine and coronary artery disease (CAD) risk among South Indians. Clinical Chimica Acta 405 (2009) 127-131
Angalena R, Ajay Chaudhary, Murali D Bashyam, Ashwin Dalal. Hemoglobin D (Iran) masquerading as Hemoglobin E: An interesting case report. Newsletter of Genetics Chapter of Indian Academy of Pediatrics, Vol 2, Issue 1 (Jan-Mar 2009)
Hypertrichosis, hyperkeratosis and mental retardation syndrome: further delineation of phenotype.Link. Dalal A, Mehrotra RN. Clin Dysmorphol. 2009 Apr;18(2):83-4.
Pradhan Mandakini, Dalal Ashwin B, Kapoor Aditya, Kumar Sudeep, Manisha R. Fetal left ventricular diverticulum presenting as dysrhythmia: diagnosis and management. Fetal Diagnosis and Therapy 2007;23(1):10-14.Link
Phadke Shubha R, Dalal Ashwin B Short stature with absent carpals and joint contractures - a new syndrome. Clinical Dysmorphology 2007;16(1):55-57. Link
Dalal Ashwin B, Phadke Shubha R. Morphometric analysis of face in dysmorphology. Computer programs and methods in biomedicine 2007; 85(2):165-7. Link
Ashwin Dalal, Shubha R Phadke. Twin pregnancy with Roberts syndrome in one fetus and trisomy 18 in other. Journal of Clinical Ultrasound 2006; 34(3): 146-149. Link
Mandakini Pradhan, Ashwin Dalal, Manisha, Niraj Kumari, Narendra Krishnani, Janak Kishore. Urorectal septal malformation presenting as non immune hydrops fetalis. Prenatal diagnosis 2006; 26 (6): 582-584.Link
Dalal Ashwin B, Phadke Shubha R, Pradhan Mandakini, Sharda Sheetal. Hemihyperplasia syndromes: A review of 17 cases. Indian Journal of Pediatrics 2006; 73(7): 609-615.Link
Shubha Phadke, Girisha KM, Ashwin Dalal. Handless footless fetus. Clin Dysmorph 2006; 15(4):233-234. Link
Ashwin Dalal, Mandakini Pradhan, Deepshikha Tiwari, Sanjay Behari, Rajkumar, Uttam Singh, G K Mallik, Vinita Das, Sarita Agarwal. MTHFR 677C-T and 1298A-C Polymorphisms: Evaluation of Maternal Genotypic Risk and Association with Level of Neural Tube Defect Gynaecologic and Obstetric Investigation 2006; 63(3), 146-150. Link
Ashwin Dalal, Deepshikha Tiwari, Satyendra Tewari, Usha Rani Gupta, Mandakini Pradhan, Nakul Sinha, Sarita Agarwal. Association of coronary artery disease with ACE and MTHFR gene polymorphism in Indian population. Indian Heart Journal 2006; 58:1-6. Link
Ashwin Dalal, Mandakini Pradhan & Sarita Agarwal. Genetics of bleeding disorders. Indian journal of Human Genetics 2006; 6(1):27-32. Link
Mandakini Pradhan, Ashwin Dalal, Faisal Khan, Suraksha Agrawal. Fertility in men with Down syndrome: a case report. Fertility and Sterility 2006; 86(6).e1-3. Link
Ashwin Dalal, Mandakini Pradhan. Not a rare case of "Cyclops with hydrocephaly" but a case of Holoprosencephaly. J Obstet Gynaecol India 2006; 56 (1): 85. (Letter to editor)
Ashwin Dalal, M P Silveira. Immunization status of children in Goa. Indian Pediatrics. 2005; 42: 401-402. Link
Ashwin Dalal, Shubha R Phadke. MTHFR polymorphisms in neural tube defects: Current perspective. Journal of Metabolism and Genetics 2005; 1(2): 109-115.
Ashwin Dalal, Shubha R Phadke. A Case of Hemihyperplasia with Ehlers- Danlos Syndrome like Skin Changes. Clin Dysmorph 2005; 14(4): 207-208.Link
Renu Singh, Shubha Phadke, M Pradhan, Ashwin Dalal (2004). Unexpected chromosomal abnormalities at prenatal diagnosis: A counseling dilemma. Perinatology 2004; 6(6): 305-309.
Sankar V H, Ashwin B Dalal, M Pradhan, Sarita Agarwal. (2004) Thalassemia intermedia: An Overview, in Recent advances in genetics and health, Osmania University, 63-77.
|Last updated on : Friday, 5th April, 2013.