Zoekresultaten - "Consanguinity"

Association between adverse pregnancy outcomes and preceding risk factors: a cross-sectional study from Nashik District, India door Prakash Prabhakarrao Doke, Sonali Hemant Palkar, Jayashree Sachin Gothankar, Archana Vasantrao Patil, Amruta Paresh Chutke, Prasad Dnyandeo Pore, Aniruddha Vinayakrao Deshpande, Khanindra Kumar Bhuyan, Madhusudan Vamanrao Karnataki, Aparna Nishikant Shrotri

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Risk Factors of Attention Deficit Hyperactivity Disorder in Children door Katayoun Khoushabi, Ameneh Setareh-Forouzan, Shahram Moradi, Parvaneh Mohammadkhani

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Socio- Cultural Variables Of Congenital Malformation In Newborns door Khan Zulfia, Pattnayak U, Ahmed A.J, Zaheer M

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Atypical Mal de Meleda in a Hispanic Patient door Mónica Guevara, Michelle Mafla, Camila Miño

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Risk indicators of aggressive periodontitis in a Jordanian population door Khansa T. Ababneh, Manal J. Maslamani, Muna S. Abbadi, Anas H. Taha, Jumana A. Karasneh, Amani G. Sa'di, Yousef S. Khader

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Incidence of and Maternal-fetal Risk Factors Associated with Therapeutic Abortion: A Nested Case-control Design Based on a Population-based Historical Cohort door Zahra Maleki, Haleh Ghaem, Mozhgan Seif, Sedigheh Foruhari

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Etiologies of Childhood Hearing Impairment in Schools for the Deaf in Mali door Abdoulaye Yalcouyé, Abdoulaye Yalcouyé, Oumou Traoré, Abdoulaye Taméga, Alassane B. Maïga, Fousseyni Kané, Oluwafemi G. Oluwole, Cheick Oumar Guinto, Cheick Oumar Guinto, Mohamed Kéita, Mohamed Kéita, Samba Karim Timbo, Samba Karim Timbo, Carmen DeKock, Guida Landouré, Guida Landouré, Ambroise Wonkam, Ambroise Wonkam

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A clinical study of retinoblastoma door L Subha, Arun Subhash Reddy, Ramyaa

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Case report: Artemis deficiency and 3M syndrome-coexistence of two distinct genetic disorders door Ayca Ceylan, Ilyas Emre Tekdemir, Nadir Kocak, Ivan Kingyue Chinn, Jordan Scott Orange, Hasibe Artac

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Application of next generation sequencing in genetic counseling a case of a couple at risk of cystinosis door Mouna Ouhenach, Abdelali Zrhidri, Imane Cherkaoui Jaouad, Wiam Smaili, Abdelaziz Sefiani

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Frequency of Congenital Anomalies in the Brazilian Midwest and the Association with Maternal Risk Factors: Case-control Study door Carolina Leão de Moraes, Natália Cruz e Melo, Waldemar Naves do Amaral

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Survey of cutaneous findings in newborns in Saudi Arabia door Fatimah Budair, Salih Aljabre, Nada Alquorain, Norah Alnafea, Abdullah Aljabre, Abdullah Alburaey

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MATERNAL RISK FACTORS FOR INTRAUTERINE FETAL DEATH (IUFD) door Ghyiacy, P, Jahanfar, Sh, Mokhtar Shahy, Sh, Haghani, H

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Two mutations in the thiazide-sensitive NaCl co-transporter gene in a Romanian Gitelman syndrome patient: case report door Gug C, Mihaescu A, Mozos I

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Genome-wide analysis of runs of homozygosity in Pakistani controls with no history of speech or language-related developmental phenotypes door Tahira Yasmin, Erin M. Andres, Komal Ashraf, Muhammad Asim Raza Basra, Muhammad Hashim Raza

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Three Siblings with Cohen Syndrome and a Novel Vacuolar Protein Sorting 13 Homolog B Mutation door Naseer Yousuf Mir, Altaf Hussain, Khurshid Ahmad Wani, Sanjeet Singh, Ummar M Bhat

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Factors Affecting the Willingness to Undertake Premarital Screening Test Among Prospective Marital Individuals door Ali Alkalbani RN, Maryam Alharrasi PhD, RN, Susan Achura MSN, RN, Ammar Al Badi RN, Amjad Al Rumhi RN, Khalid Alqassabi RN, Raya Almamari MSN student, RN, Omar Alomari PhD, RN

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Phenotypic and Genetic Characterization of a Cohort of Pediatric Wilson Disease Patients door Elnaghy Suzan, Elsayed Solaf M, Abdel Ghaffar Tawhida Y, Shadeed Ahmed, Elsobky Ezzat S, Schmidt Hartmut

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Epidemiology of Phenylketonuria Disease in Jordan: Medical and Nutritional Challenges door Safwan Dababneh, Mohammed Alsbou, Nashat Taani, Ghazi Sharkas, Refqi Ismael, Latifeh Maraqa, Omar Nemri, Hanin Al-Jawaldeh, Nadeen Kopti, Enas Atieh, Arab Almasri

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Family Aggregation in Individuals with Essential Arterial Hypertension and Risk Factors door Julio Armando Sánchez Delgado, Nailé Edita Sánchez Lara

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