Indian Journal of Human Genetics
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scholarly journals FLT3 and NPM-1 mutations in a cohort of acute promyelocytic leukemia patients from India

2014 ◽  
Vol 20 (2) ◽  
pp. 160 ◽  
Author(s):  
Kanjaksha Ghosh ◽  
Suchitra Swaminathan ◽  
Swati Garg ◽  
Manisha Madkaikar ◽  
Maya Gupta ◽  
...  
Keyword(s):  
Acute Promyelocytic Leukemia ◽  
Promyelocytic Leukemia

scholarly journals Omphalocele, exstrophy of cloaca, imperforate anus and spinal defect (OEIS Complex) with overlapping features of body stalk anomaly (limb body wall complex)

2014 ◽  
Vol 20 (2) ◽  
pp. 195 ◽  
Author(s):  
SureshR. S. Mandrekar ◽  
Sangeeta Amoncar ◽  
Siddhartha Banaulikar ◽  
Vishal Sawant ◽  
R. G. W. Pinto
Keyword(s):  
Imperforate Anus ◽  
Body Wall

scholarly journals Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with down-syndrome like facies

2014 ◽  
Vol 20 (1) ◽  
pp. 89 ◽  
Author(s):  
Abdelhafid Natiq ◽  
SihamChafai Elalaoui ◽  
Thomas Liehr ◽  
Saïd Amzazi ◽  
Abdelaziz Sefiani
Keyword(s):  
Down Syndrome ◽  
Chromosome 22

scholarly journals Wildervanck syndrome with hypoplastic frontal sinus: A rare case presentation

2014 ◽  
Vol 20 (2) ◽  
pp. 189 ◽  
Author(s):  
SuwanshSukhadeorao Meshram ◽  
Sheetal Nikose ◽  
Shraddha Jain ◽  
Amar Taksande
Keyword(s):  
Frontal Sinus ◽  
Rare Case ◽  
Case Presentation

scholarly journals Chronic myeloid leukemia in case of Klinefelter syndrome

2014 ◽  
Vol 20 (1) ◽  
pp. 69 ◽  
Author(s):  
Rajesh Kashyap ◽  
Parag Tamhankar ◽  
Subha Phadke ◽  
Vasundhara Chennuri
Keyword(s):  
Chronic Myeloid Leukemia ◽  
Myeloid Leukemia ◽  
Klinefelter Syndrome
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