Arama Sonuçları - "normal family"

Clinical and genetic analysis of two phenotypically normal families carrying 4p16.1 microduplications Yazar: Xiaolin Wang, Yujiao Wang, Xinqiang Lan

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My home - the hospital: A case study Yazar: D.D. Jaftha

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Analysis of TYR gene pathogenic variants in a Chinese Mongolian family with progressive symmetric erythrokeratoderma Yazar: Yan Duan, Linye Li, Yue He, Jian Wang

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Constructing of "marital I". A family as a space of spouses' support and learning equality Yazar: Joanna Ostrouch-Kamińska

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The Study of the Role of Contributor Factors in Addiction Withdrawal Yazar: Omar Kianipour, Akram Pouzad

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Women, Sport and Baby-is it possible to do/have all? Yazar: Robert Kuchar

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Physical Activity Level, Mediterranean Diet Adherence, and Emotional Intelligence as a Function of Family Functioning in Elementary School Students Yazar: Eduardo Melguizo-Ibáñez, Virginia Viciana-Garófano, Félix Zurita-Ortega, José Luis Ubago-Jiménez, Gabriel González-Valero

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Family life of caregivers: A descriptive study of disruption of family activities, leisures and interaction of caregivers of children with cerebral palsy Yazar: Ramita Sardana, U. Singh, K.B. Sumalatha

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Case-Based Insights: Arab Muslim Mothers' Experiences of Managing a Child Newly Diagnosed With Type 1 Diabetes Mellitus Yazar: Rachel Cathrine Rossiter HlthScD, Jennifer Louise Cooper DPubHlth, Suhad Issa Marjei BSN, Sharon Brownie DBA

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A novel <it>DSPP </it>mutation is associated with type II dentinogenesis Imperfecta in a chinese family Yazar: Xu Chengqi, Wang Xiaotao, Chang Wei, Zhao Zhen, Qu Erjun, Chen Lanying, Liu Jingyu, Zhang Xianqin, Wang Qing K, Liu Mugen

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Impact of the Poor Oral Health Status of Children on Their Families: An Analytical Cross-Sectional Study Yazar: Mir Faeq Ali Quadri, Fatimah Rasheed M. Jaafari, Noha Ahmed A. Mathmi, Nouf Hassan F. Huraysi, Maryam Nayeem, Abbas Jessani, Santosh Kumar Tadakamadla, Jyothi Tadakamadla

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Experiences of Being a Parent to a Child with Amelogenesis Imperfecta Yazar: Gunilla Pousette Lundgren, Tove Hasselblad, Anna Stigsdotter Johansson, Anna Johansson, Göran Dahllöf

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"The Logic of Care" - Parents' perceptions of the educational process when a child is newly diagnosed with type 1 diabetes Yazar: Jönsson Lisbeth, Hallström Inger, Lundqvist Anita

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De lo invisible y lo cotidiano. Familias y discapacidad / The invisible and the daily. Families and discapacity Yazar: Sandra Araya Umaña

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Identification of a novel <it>KCNQ1 </it>mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family Yazar: Liu Jing, Yang Junguo, Cheng Lingling, Zhang Shirong, Wang Pengyun, Ren Xiang, Yin Ke, Zhang Su, Liu Mugen, Wang Qing

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De novo variation in EP300 gene cause Rubinstein-Taybi syndrome 2 in a Chinese family with severe early-onset high myopia Yazar: Xiaoyu Huang, Xue Rui, Shuang Zhang, Xiaolong Qi, Weining Rong, Xunlun Sheng

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Fighting the waves; Covid-19 family life interference in a neurodevelopmental disorder-caregiver population Yazar: Mats Nylén-Eriksen, Mariela Loreto Lara-Cabrera, Ellen Karine Grov, Hanne Skarsvaag, Irene Lie, Tone Dahl-Michelsen, Torill Margaret Sæterstrand, Arthur Mandahl, Hege Hafstad, Mona Breding Lersveen, Ann Kristin Bjørnnes

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Novel mutations of the X-linked genes associated with early-onset high myopia in five Chinese families Yazar: Feiyin Zi, Zhen Li, Wanyu Cheng, Xiaoyu Huang, Xunlun Sheng, Weining Rong

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De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia Yazar: Xiaoyu Huang, Huiping Li, Shangying Yang, Meijiao Ma, Yuanyuan Lian, Xueli Wu, Xiaolong Qi, Xuhui Wang, Weining Rong, Xunlun Sheng

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Effect of family type on depression symptoms among high school students in Jiangsu province: a cross-sectional survey with propensity score matching analysis Yazar: Wenyi YANG, Yonglin ZHOU, Yan WANG, Yanjun CHEN, Xiyan ZHANG, Jingyang ZHANG, Yiliang XIN, Jie YANG

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