Volume 18; Issue 3

Indian Journal of Human Genetics

Volume 18; Issue 3

1

Small players with a big role: MicroRNAs in pathophysiology of cleft lip and palate

Radhakrishna, Uppala

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 196 KB

english, 2012

2

Redefining the potential applications of dental stem cells: An asset for future

Rai, Shalu, Kaur, Sandeep, Kaur, Mandeep, Arora, SapnaPanjwani

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 528 KB

english, 2012

3

The use of hormones indicators in human saliva in diagnosing parodontitis in pregnant women

Zukow, W, Atmazhov, ID, Muszkieta, R, Skaliy, A, Dolomatov, SI

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 255 KB

english, 2012

4

Pharmacogenetic typing for oral anti-coagulant response among factor V Leiden mutation carriers

Verma, IshwarC, Nahar, Risha, Saxena, Renu, Deb, Roumi

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 393 KB

english, 2012

5

Genetic significance of muscle segment homeo box1 gene in South Indian population for cleft lip and palate

Venkanna, SPrasad, Shivani, Venkatesh

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 312 KB

english, 2012

6

Rhizomelic chondrodysplasia punctata: A missed opportunity for early diagnosis

Venkatesh, Chandrasekaran, Karthikeyan, Kadirvel, Chhavi, Nanda, Prashanth, Sankar

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 489 KB

english, 2012

7

An uncommon case of an adult with del(5)(q) in acute lymphoblastic leukemia

Prasannakumari,, Venkataswamy, E, Nargund, AshwiniR, Prabhudesai, Shilpa, Patil, GeetaV, Rao, JChandra, Veldore, VidyaH, Patil, Shekar, Verma, Amit, Sahoo, Rashmita, Ajaikumar, BS

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 333 KB

english, 2012

8

A new 48, XXYY/47, XYY syndrome associated with multiple skeletal abnormalities, congenital heart disease and mental retardation

Mutesa, Leon, Jamar, Mauricette, Hellin, AnneCecile, Pierquin, Genevieve, Bours, Vincent

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 751 KB

english, 2012

9

Renal amyloidosis due to familial Mediterranean fever misdiagnosed

Hama, Iman, Ilham, Ratbi, Ouzeddoun, Naima, Alhamany, Zaitouna, Bayahia, Radia, Sefiani, Abdelaziz

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 305 KB

english, 2012

10

Seven nipples in a male: World′s second case report

Goyal, Tarang, Bakshi, SK, Varshney, Anupam

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 431 KB

english, 2012

11

Orofaciodigital syndrome type-VI (Varadi-Papp syndrome) with several Y-shaped metacarpals

Mahato, PulakR, Pandey, ShashiB

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 393 KB

english, 2012

12

Chronic pancreatitis: A new pathophysiology

Agarwal, Sarita, Singh, Shweta, Kumar, Ravindra, Choudhuri, Gourdas

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 353 KB

english, 2012

13

Analysis of loss of heterozygsity effect on thyroid tumor with oxyphilia cell locus in familial non medullary thyroid carcinoma in Iranian families

Azizi, Fereidoun, Shirazi, HastiAtashi, Hedayati, Mehdi, Daneshpour, MaryamSadat, Shafiee, Abdollah

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 693 KB

english, 2012

14

Vitamin D receptor and type 2 diabetes mellitus: Growing therapeutic opportunities

Bid, HemantK, Manchanda, ParmeetKaur

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 917 KB

english, 2012

15

Octaploidy in idiopathic thrombocytopenia purpura: Is it incidental or causal?

Vundinti, BabuRao, Vaidya, Shantashri

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 195 KB

english, 2012

16

Conditional deletion of the human ortholog gene Dicer1 in Pax2-Cre expression domain impairs orofacial development

Rocha-Sanchez, SoniaM, Barritt, LauraC, Miller, JosephM, Scheetz, LauraR, Gardner, Kelsey, Pierce, MarshaL, Soukup, GarrettA

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 2.94 MB

english, 2012

17

Annoucement

Ghosh, Kanjaksha

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 169 KB

english, 2012

18

Proteus syndrome: A rare case report

Subbanna, Praveen KumarArinaganhalli, Amalnath, Deepak, Krishna Suri, SubrahmanyamDharanitragada, Talari, Keerthi

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 638 KB

english, 2012

19

A new syndrome with overlapping features of Townes-brocks syndrome and single median maxillary central incisor syndrome

Babu, ThirunavukkarasuArun, Chandrasekaran, Venkatesh, Balachandran, Sathish

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 795 KB

english, 2012

20

Novel mutation in an Indian patient with Methylmalonic Acidemia, cblA type

Girisha, KattaMohan, Shrikiran, Aroor, Sakamoto, Osamu, Gopinath, PuthiyaMundyat, Satyamoorthy, Kapaettu, Bidchol, AbdulMueed

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 597 KB

english, 2012

21

Hemoglobinopathies in South Gujarat population and incidence of anemia in them

Gupte, SnehalataC, Patel, AnkurG, Shah, AvaniP, Sorathiya, SmitaM

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 251 KB

english, 2012

22

Analysis of autosomal dominant spinocerebellar ataxia type 1 in an extended family of central India

Tiwari, PramodKumar, Sharma, Shashikant, Singh, TekchamDinesh, Poojary, SatishS, Rohilla, ManojSingh, Singh, Ajaypal, Lowalekar, KishoreB

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 662 KB

english, 2012

23

A case of oligoasthenoteratozoospermia with AZFc deletion and persistent oxidative stress

Singh, Rajender, Kaleem, AhmadMohammad, Narayana, SankhwarSatya, Mahdi, AbbasAli

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 359 KB

english, 2012

24

Evaluation of C677T polymorphism of the methylenetetra hydrofolate reductase gene and its association with levels of serum homocysteine, folate, and vitamin B12 as maternal risk factors for Down syndrome

Mohanty, PankajK, Kapoor, Seema, Dubey, AnandP, Pandey, Sanjeev, Nayak, HemantK, Polipalli, SunilK, Shah, Renuka

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 271 KB

english, 2012

25

The low frequency of Y chromosome microdeletions in subfertile males in a Sinhalese population of Sri Lanka

Dissanayake, VajiraH. W., Wettasinghe, TithilaKalum, Jayasekara, RohanW

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 593 KB

english, 2012

26

Molecular analysis of exons 6 and 7 of phenylalanine hydroxylase gene mutations in Phenylketonuria patients in Western Iran

Alibakhshi, Reza, Ghadiri, Keyghobad, Khatami, SaeidReza, Galehdari, Hamid, Moradi, Keyvan

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 247 KB

english, 2012

27

A novel 11;18 translocation in a case of acute myeloid leukemia with maturation

Devi, GSandhya, Ahmed, Faiq, Khadke, Kavita, Murthy, SudhaS, Rajappa, SenthilJ

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 969 KB

english, 2012

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