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Journal Article
Australian Journal of Electrical and Electronics Engineering, ISSN 1448-837X, 10/2017, Volume 14, Issue 3-4, pp. 88 - 92
In this paper, an optimised Long-Term Evolution (LTE) system model using advanced modulation schemes and equalisation techniques is presented. This new... 
OLSM | LTE | CLSM | MMSE
Journal Article
Indian dermatology online journal, ISSN 2229-5178, 09/2017, Volume 8, Issue 5, pp. 352 - 354
Autosomal recessive cutis laxa type-II (ARCLII) is a spectrum of clinical disorders with prenatal and postnatal growth retardation, cutis laxa, dysmorphism,... 
dysmorphism | Autosomal recessive cutis laxa | novel mutation | Case Report
Journal Article
Journal Article
Journal of Pediatric Genetics, ISSN 2146-4596, 06/2013, Volume 2, Issue 2, pp. 109 - 112
Abstract Fanconi-Bickel syndrome is a rare autosomal-recessive disorder caused by defects in the facilitative glucose transporter 2 ( GLUT2 ) gene. It is... 
Case Report | Fanconi-Bickel syndrome | Hypophosphatemic rickets | Glycogen storage disease type XI | glycogen storage disease type XI | hypophosphatemic rickets
Journal Article
Case reports in genetics, ISSN 2090-6544, 2011, Volume 2011, pp. 839650 - 4
There are multiple genetic disorders with known or unknown etiology grouped under obesity syndromes. Inspite of having multisystem involvement and often having... 
Case Report
Journal Article
Journal of Pediatric Endocrinology and Metabolism, ISSN 0334-018X, 01/2014, Volume 27, Issue 1, pp. 185 - 188
Journal Article
Journal Article
Journal of Pediatric Genetics, ISSN 2146-4596, 01/2013, Volume 2, Issue 2, pp. 109 - 112
Fanconi-Bickel syndrome is a rare autosomal-recessive disorder caused by defects in the facilitative glucose transporter 2 (GLUT2) gene. It is characterized by... 
Journal Article
Pediatric Dermatology, ISSN 0736-8046, 01/2010, Volume 27, Issue 1, pp. 43 - 47
:  Crouzon syndrome is a craniosynostosis syndrome, characterized by cloverleaf skull, hypertelorism, exophthalmos, external strabismus, parrot‐beaked nose,... 
PEDIATRICS | ALA391GLU | FGFR3 | MUTATION | DERMATOLOGY | Craniofacial Dysostosis - pathology | Acanthosis Nigricans - pathology | Biopsy | Humans | Facies | Acanthosis Nigricans - complications | Male | Infant, Newborn | Skin - pathology | Craniofacial Dysostosis - complications | Acanthosis nigricans
Journal Article
The Indian Journal of Pediatrics, ISSN 0019-5456, 7/2006, Volume 73, Issue 7, pp. 609 - 615
Hemihyperplasia is a heterogenous group of disorders characterized by asymmetric limb growth. There is considerable confusion regarding their classification... 
Pediatrics | Hemihyperplasia | Proteus | Medicine & Public Health | Gynecology | Overgrowth | Syndrome | Humans | Adolescent | Growth Disorders - diagnosis | Child, Preschool | Female | Infant | Male | Extremities - growth & development | Child
Journal Article
Journal of Pediatric Orthopaedics, ISSN 0271-6798, 03/2007, Volume 27, Issue 2, pp. 225 - 227
Journal Article
Journal of Pediatric Hematology/Oncology, ISSN 1077-4114, 10/2009, Volume 31, Issue 10, pp. 766 - 767
Journal Article
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