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Genetic Counseling (Geneva, Switzerland)|February 26, 2013
A patient with 9q subtelomeric deletion syndrome with additional findingsE Tug, B Cavdarli, M Yirmibes Karaoguz, et al.
Genetic Counseling (Geneva, Switzerland)|February 26, 2013
Severe rhizomelic chondrodysplasia punctata in a fetus due to maternal mixed connective tissue disorderS S Nayak, P K Adiga, L Rai, et al.
Genetic Counseling (Geneva, Switzerland)|February 26, 2013
Analysis of the genes encoding neuroligins NLGN3 and NLGN4 in Bulgarian patients with autismD M Avdjieva-Tzavella, T P Todorov, A P Todorova, et al.
Genetic Counseling (Geneva, Switzerland)|December 18, 2013
Crigler-Najjar syndrome type I in a Turkish newborn caused by a novel mutation and Gilbert type genetic defectD Yildiz, S Alan, A Kilic, et al.
Genetic Counseling (Geneva, Switzerland)|December 18, 2013
Bamforth syndrome: is porencephaly a new finding?G Sandal, O Pirgon, A R Ormeci
Genetic Counseling (Geneva, Switzerland)|December 3, 2015
ASSOCIATED NON DIAPHRAGMATIC ANOMALIES AMONG CASES WITH CONGENITAL DIAPHRAGMATIC HERNIAC Stoll, Y Alembik, B Dott, et al.
Genetic Counseling (Geneva, Switzerland)|February 9, 2016
RECURRENT RAB3GAP1 MUTATIONS IN THE TURKISH POPULATIONS Tasdemir, I Sahin, D J Morris-Rosendahl, et al.
Genetic Counseling (Geneva, Switzerland)|May 20, 2016
CLINICAL FEATURES AND GENETIC ANALYSIS OF SIX PATIENTS WITH WISKOTT-ALDRICH SYNDROME REPORTING TWO NOVEL MUTATIONS: EXPERIENCE OF ERCIYES UNIVERSITY, KAYSERI, TURKEYT Patiroglu, C Klein, H Eke Gungor, et al.
Genetic Counseling (Geneva, Switzerland)|May 20, 2016
22.5 MB DELETION OF 13q31.1-q34 ASSOCIATED WITH HPE, DWM, AND HSCR: A CASE REPORT AND REDEFINING THE SMALLEST DELETED REGIONSM Y Alp, A H Çebi, S Seyhan, et al.
Genetic Counseling (Geneva, Switzerland)|February 22, 2008
A theoretical psychological perspective on predictive testing for late onset hereditary diseasesE Mularczyk, M Decruyenaere, L Denayer, et al.
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