Search Results - "Normal family

Novel GNAI3 mutation in a Chinese family with auriculocondylar syndrome and treatment of severe dentofacial deformities: a 5-year follow-up case report by Yulin Shi, Liang Rong, Siying Liu, Yiwen Liu, Chunlin Zong, Jinbiao Lu, Hongtao Shang, Yang Xue, Lei Tian

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The Effect of Entrepreneurship Achievement and Family Economic on Entrepreneurship Interest of XII Automotive Grade Students SMK Taman Karya Madya Jetis Yogyakarta Year 2013/2014 by Tri Kurniawan Krisbowo

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A family-based intervention targeting parents of preschool children with overweight and obesity: conceptual framework and study design of LOOPS- Lund overweight and obesity prescho... by Önnerfält Jenny, Erlandsson Lena-Karin, Orban Kristina, Broberg Malin, Helgason Christina, Thorngren-Jerneck Kristina

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Society, family, and individual characteristics as double-edged swords in the social reintegration of Iranian female survivors from unintentional severe burns: a qualitative study... by Masumeh Hemmati Maslakpak, Fardin Ajoudani, Mojgan Lotfi, Vahid Alinejad

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Challenges in medical education: the Family Health Program as educational practice Desafios na formação médica: o Programa Saúde da Família como prática de ensino by Eluiza Helena Leite Arias

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Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasound by Chih-Ping Chen, Jian-Pei Huang, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Wayseen Wang, Chen-Chi Lee

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Impact of prepregnancy body mass index on adverse pregnancy outcomes: analysis from the Longitudinal Indian Family hEalth cohort studyAJOG MFM at a Glance by Monica Gudipally, MD, Fouzia Farooq, PhD, MPH, Kalpana Basany, MD, Catherine L. Haggerty, PhD, MPH, Gong Tang, PhD, Govindrao N. Kusneniwar, MD, Guru Rajesh Jammy, PhD, MPH, Clareann H. Bunker, PhD, P.S. Reddy, MD

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A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani family by Anwar Kamal Khan, Noor Muhammad, Abdul Aziz, Sher Alam Khan, Khadim Shah, Abdul Nasir, Muzammil Ahmad Khan, Saadullah Khan

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PENGARUH BEBAN KERJA DAN WORK FAMILY CONFLICT MELALUI WORK LIFE BALANCE SEBAGAI VARIABEL INTERVENING TERHADAP TURNOVER INTENTION KARYAWAN SHOPEE DI JAKARTA by Fadilla Azahra Suhendar,

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Body Mass Index Asian populations category and stroke and heart disease in the adult population: a longitudinal study of the Indonesia Family Life Survey (IFLS) 2007 and 2014 by Kamaluddin Latief, Dieta Nurrika, Min-Kuang Tsai, Wayne Gao

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A novel splice-altering TNC variant (c.5247A > T, p.Gly1749Gly) in an Chinese family with autosomal dominant non-syndromic hearing loss by Min He, Miaomiao Hu, Qiang Zhang, Kai Yao

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Masa ciała dzieci uczących się w podstawowych szkołach wiejskich a styl życia rodzin = The body weight of rural primary school pupils and the lifestyle of their families by Zdzisława Szadowska-Szlachetka, Magdalena Tarka, Barbara Ślusarska, Marta Łuczyk, Agata Pietraszek, Robert Łuczyk, Agnieszka Bartoszek, Marianna Charzyńska-Gula

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Masa ciała dzieci uczących się w podstawowych szkołach wiejskich a styl życia rodzin = The body weight of rural primary school pupils and the lifestyle of their families by Zdzisława Szadowska-Szlachetka, Magdalena Tarka, Barbara Ślusarska, Marta Łuczyk, Agata Pietraszek, Robert Łuczyk, Agnieszka Bartoszek, Marianna Charzyńska-Gula

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Perceptions and attitudes of family medicine residency program directors regarding ranking applicants for residency programs using their social media accounts: A national study in... by Amani M Al Qarni, Shaher Z Al Shehri, Moataza M.A. Wahab

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Chapter Remote working in Italy: Just a pandemic accident or a lesson for the future? by Bollani, Luigi

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Chapter Remote working in Italy: Just a pandemic accident or a lesson for the future? by Bollani, Luigi

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A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients by Sibtain Afzal, Khushnooda Ramzan, Sajjad Ullah, Salma M. Wakil, Arshad Jamal, Sulman Basit, Ahmed Bilal Waqar

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Identification of de novo mutations for ARID1B haploinsufficiency associated with Coffin-Siris syndrome 1 in three Chinese families via array-CGH and whole exome sequencing by Guanting Lu, Qiongling Peng, Lianying Wu, Jian Zhang, Liya Ma

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The Association between MUC5B Rs35705950 and Risks of Idiopathic Interstitial Pneumonia, Systemic Sclerosis Interstitial Lung Disease, and Familial Interstitial Pneumonia: A Meta... by Huai-qing LUO, Chun-Xia HUANG, Guang-Yi LI, Ping LI, Shou-Ming ZHANG, Hai-Gang LI, Li HAN, Mei-Hua BAO

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The association of body mass index and its interaction with family history of dyslipidemia towards dyslipidemia in patients with type 2 diabetes: a cross-sectional study in Zhejian... by Xiang-Yu Chen, Le Fang, Jie Zhang, Jie-Ming Zhong, Jing-Jing Lin, Feng Lu

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