Cytogenetic and Morphological Analysis of De Novo Acute Myeloid Leukemia in Adults: A Single Center Study in Jordan

por Ayesh, MH, Khassawneh, B, Matalkah, I, Alawneh, K, Jaradat, S
Publicado 2012

Clouston Syndrome: First Case in Russia

por Marakhonov, AV, Skoblov, MYu, Galkina, VA, Zinchenko, RA
Publicado 2012

Influence of the SCN1A IVS5N + 5 G>A Polymorphism on Therapy with Carbamazepine for Epilepsy

por Sterjev, Z, Kiteva, G, Cvetkovska, E, Petrov, I, Kuzmanovski, I, Ribarska, TJ, Nestorovska, KA, Matevska, N, Trajkovik-Jolevska, S, Dimovski, AJ, Suturkova, Lj
Publicado 2012

CAG Repeat Number in the Androgen Receptor Gene and Prostate Cancer

por Madjunkova, S, Eftimov, A, Georgiev, V, Petrovski, D, Dimovski, AJ, Plaseska-Karanfilska, D
Publicado 2012

Rapid Detection of Fetal Aneuploidies by Quantitative Fluorescent-Polymerase Chain Reaction for Prenatal Diagnosis in the Turkish Population

por Guzel, AI, Yilmaz, MB, Demirhan, O, Pazarbasi, A, Kocaturk-Sel, S, Erkoc, MA, Inandiklioglu, N, Ozgunen, FT, Sariturk, C
Publicado 2012

Mitochondrial DNA 4977 bp Deletion in Chronic Cervicitis and Cervix Cancers

por Kara, M, Tatar, A, Borekci, B, Dagli, F, Oztas, S
Publicado 2012

The Many Faces of Oral-Facial-Digital Syndrome

por Sukarova-Angelovska, E, Angelkova, N, Palcevska-Kocevska, S, Kocova, M
Publicado 2012

Muscle Hemangiomatosis Presenting as a Severe Feature in a Patient with the Pten Mutation: Expanding the Phenotype of Vascular Malformations in Bannayan-Riley-Ruvalcaba Syndrome

por Soysal, Y, Acun, T, Lourenço, CM, Marques, W, Yakıcıer, MC
Publicado 2012

Mosaic Intrachromosomal Triplication of (12)(p11.2p13) in a Patient with Pallister-Killian Syndrome

por Yakut, S, Mihci, E, Altiok Clark, O, Cetin, Z, Keser, I, Berker, S, Luleci, G
Publicado 2012

Ring Chromosome 22: A Review of the Literature and First Report from India

por Mahajan, S, Kaur, A, Singh, JR
Publicado 2012

The Impact of the D727E Polymorphism has no Significant Role in Multi Nodular Goiter

por Tug, E, Sengül, N, Aydin, H, Yilmaz, EE
Publicado 2012

Mitochondrial DNA Mutations in Two Bulgarian Children with Autistic Spectrum Disorders

por Avdjieva-Tzavella, D, Mihailova, S, Lukanov, C, Naumova, E, Simeonov, E, Tincheva, R, Toncheva, D
Publicado 2012

Chromosomal Polymorphisms Involved in Reproductive Failure in the Romanian Population

por Mierla, D, Stoian, V
Publicado 2012

Detecting Sex-Biased Gene Flow in African-Americans through the Analysis of Intra- and Inter-Population Variation at Mitochondrial DNA and Y- Chromosome Microsatellites

por Battaggia, C, Anagnostou, P, Bosch, I, Brisighelli, F, Destro-Bisol, G, Capocasa, M
Publicado 2012

Human Leukocyte Antigen-B27 and Disease Susceptibility in Vojvodina, Serbia

por Vojvodić, S, Ademović-Sazdanić, D, Busarčević
Publicado 2012

Association between Obsessive Compulsive Disorder and Tumor Necrosis Factor-α Gene −308 (G>A) and −850 (C>T) Polymorphisms in Turkish Children

por Lüleyap, HU, Onatoğlu, D, Tahiroğlu, AY, Alptekin, D, Yılmaz, MB, Çetiner, S, Pazarbaşı, A, Ünal, İ, Avcı, A
Publicado 2012

Cytogenetic Findings in Mentally Retarded Iranian Patients

por Nasiri, F, Mahjoubi, F, Manouchehry, F, Razazian, F, Mortezapour, F, Rahnama, M
Publicado 2012

Ring Autosomes: Some Unexpected Findings

por Caba, L, Rusu, C, Plăiaşu, Gug, G, Grămescu, M, Bujoran, C, Ochiană, D, Voloşciuc, M, Popescu, R, Braha, E, Pânzaru, M, Butnariu, L, Sireteanu, A, Covic, M, Gorduza, EV
Publicado 2012

Clinical Impact of Proximal Autosomal Imbalances

por Hamid, AB, Weise, A, Voigt, M, Bucksch, M, Kosyakova, N, Liehr, T, Klein, E
Publicado 2012

16p Subtelomeric Duplication with Vascular Anomalies: an Albanian Case Report and Literature Review

por Babameto-Laku, A, Mokini, V, Kuneshka, N, Sallabanda, S, Ylli, Z
Publicado 2012