Search Results - Manisha Goyal
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1
Hypohidrotic ectodermal dysplasia with ankylosis of temporomandibular joint and cleft palate: A rare presentation by Manisha Goyal, Gaurav Pradhan, Sunita Gupta, Seema Kapoor
Published 2015Call Number: Loading…Connect to this object online.
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2
Stickler Syndrome Type 1 with Short Stature and Atypical Ocular Manifestations by Manisha Goyal, Seema Kapoor, Shiro Ikegawa, Gen Nishimura
Published 2016Call Number: Loading…Connect to this object online.
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3
The diagnostic dilemma of cutis laxa: A report of two cases with genotypic dissimilarity by Manisha Goyal, Ankur Singh, Uwe Kornak, Seema Kapoor
Published 2015Call Number: Loading…Connect to this object online.
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4
Hypohydrotic ectodermal dysplasia: A rare case series by Manisha Goyal, Ashok Gupta, Priyanshu Mathur, Manish Sharma
Published 2018Call Number: Loading…Connect to this object online.
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5
The diagnostic dilemma of rothmund-thomson syndrome Type II: A rare disorder with a novel mutation in the RECQL4 gene in an Indian Boy by Manisha Goyal, Lalit Bharadia, Ashok Gupta, Udhaya H Kotecha
Published 2022Call Number: Loading…Connect to this object online.
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6
Fetal Valproate Syndrome with Limb Defects: An Indian Case Report by Manisha Goyal, Ashok Gupta, Manish Sharma, Priyanshu Mathur, Naresh Bansal
Published 2016Call Number: Loading…Connect to this object online.
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7
An unusual presentation of Rubinstein-Taybi Syndrome with bilateral postaxial polydactyly by Pallavi Sachdeva, Priyanka Minocha, Anita Choudhary, Sadasivan Sitaraman, Manisha Goyal
Published 2016Call Number: Loading…Connect to this object online.
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8
Oro facial digital syndrome type 2- An Indian case report by Naresh Bansal, Ashok Gupta, Manisha Goyal, Manish Sharma, Priyanshu Mathur, Manish Agarwal
Published 2016Call Number: Loading…Connect to this object online.
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9
Molar Tooth Sign with Deranged Liver Function Tests: An Indian Case with COACH Syndrome by Rama Krishna Sanjeev, Seema Kapoor, Manisha Goyal, Rajiv Kapur, Joseph Gerard Gleeson
Published 2015Call Number: Loading…Connect to this object online.
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10
Newborn screening for G6PD deficiency: A 2-year data from North India by Manisha Goyal, Amit Garg, Mohan B Goyal, Somesh Kumar, Siddharth Ramji, Seema Kapoor
Published 2015Call Number: Loading…Connect to this object online.
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11
Gaucher disease: single gene molecular characterization of one-hundred Indian patients reveals novel variants and the most prevalent mutation by Jayesh Sheth, Riddhi Bhavsar, Mehul Mistri, Dhairya Pancholi, Ashish Bavdekar, Ashwin Dalal, Prajnya Ranganath, Katta M Girisha, Anju Shukla, Shubha Phadke, Ratna Puri, Inusha Panigrahi, Anupriya Kaur, Mamta Muranjan, Manisha Goyal, Radha Ramadevi, Raju Shah, Sheela Nampoothiri, Sumita Danda, Chaitanya Datar, Seema Kapoor, Seema Bhatwadekar, Frenny Sheth
Published 2019Call Number: Loading…Connect to this object online.
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