Search Results - "Brothers

Left Bundle Pacing for Left Bundle Branch Block and Intermittent Third-Degree Atrioventricular Block in a MYH7 Mutation-Related Hypertrophic Cardiomyopathy With Restrictive Phenoty... by Luyan Zhang, Xueying Cheng, Jinlong Chen, Ming Zhou, Tianwei Qian, Zhongman Zhang, Jie Yin, Han Zhang, Genyin Dai, Yuming Qin, Shiwei Yang

Connect to this object online.

Hemoglobin Agenogi - A rare abnormal beta globin chain variant by Sunita Sharma, Geetika Sharma, Jagdish Chandra, Roshan Colah

Connect to this object online.

CONSANGUINITY AND LACK OF AWARENESS; STILL A WORRISOME DILEMMA AMID THALASSEMIC FAMILIES, A CROSS-SECTIONAL STUDY by Farhat Ijaz

Connect to this object online.

Case Report: The JAK-Inhibitor Ruxolitinib Use in Aicardi-Goutieres Syndrome Due to ADAR1 Mutation by Marco Cattalini, Marco Cattalini, Jessica Galli, Jessica Galli, Fiammetta Zunica, Rosalba Monica Ferraro, Rosalba Monica Ferraro, Marialuisa Carpanelli, Simona Orcesi, Simona Orcesi, Giovanni Palumbo, Giovanni Palumbo, Lorenzo Pinelli, Silvia Giliani, Silvia Giliani, Elisa Fazzi, Elisa Fazzi, Raffaele Badolato, Raffaele Badolato

Connect to this object online.

Striving for Justice in Tony Goldwyn's Conviction Movie (2010): An Individual Psychological Perspective by RAHMAWATI, NETTY NUR

Connect to this object online

BEING A MAN OR WOMAN:A GENDER ANALYSIS OF THE NOVEL MIDDLESEXBY JEFFREY EUGENIDES by Vebyanti, -

Link Metadata

From variant of uncertain significance to likely pathogenic in two siblings with atypical RAG2 Deficiency: a case report and review of the literature by Nima Taghizadeh Mortezaei, Soha Mohammadi, Hassan Abolhassani, Sima Shokri, Mohammad Nabavi, Morteza Fallahpour, Mohammad Hassan Bemanian

Connect to this object online.

A novel mutation in TRIOBP gene leading to congenital deafness in a Chinese family by Bingxin Zhou, Lili Yu, Yan Wang, Wenjing Shang, Yi Xie, Xiong Wang, Fengchan Han

Connect to this object online.

Two cases of infantile-onset primary generalized glucocorticoid hypersensitivity and the effect of mifepristone by Xiu Zhao, Zhongwei Xu, Huiping Su, Rongfei Zheng, Min Zhan, Yuge Huang, Zhe Su

Connect to this object online.

A Case-Based Discussion Supporting Ethics Education in Medical Schools by Liliana R. Ladner, Mark G. Swope, Phyllis Whitehead

Connect to this object online.

Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorder by Chih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang

Connect to this object online.

A familial case of Blau syndrome caused by a novel genetic mutation by Woojoong Kim, Eujin Park, Yo Han Ahn, Jiwon M. Lee, Hee Gyung Kang, Byung Joo Kim, Il-Soo Ha, Hae Il Cheong

Connect to this object online.

Deixis Analysis On Richard Wright's Black Boy by An'imah, Lailati, , Dr. Phil. Dewi Candraningrum, M.Ed, , Dra. Malikatul Laila, M.Hum

Connect to this object online

Successful Hematopoietic Stem Cell Transplantation from a Matched Related Donor with Beta-Thalassemia Minor for Severe Aplastic Anemia by Mi Young Jung, Young Tae Lim, Hyunji Lim, Jeong Ok Hah, Jae Min Lee

Connect to this object online.

Central nervous system manifestations of LRBA deficiency: case report of two siblings and literature review by T. C. Mangodt, K. Vanden Driessche, K. K. Norga, N. Moes, M. De Bruyne, F. Haerynck, V. Bordon, A. C. Jansen, A. I. Jonckheere

Connect to this object online.

The trend of correlation changes of macronutrient intakes among different familial pairs: a prospective study among participants of Tehran Lipid and Glucose Study by Farshad Teymoori, Niloufar Saber, Mahdi Akbarzadeh, Hossein Farhadnejad, Ebrahim Mokhtari, Hamid Ahmadirad, Parisa Riahi, Parvin Mirmiran, Maryam S. Daneshpour, Fereidoun Azizi

Connect to this object online.

A novel COL4A5 splicing mutation causes alport syndrome in a Chinese family by Suyun Chen, Guangbiao Xu, Zhixin Zhao, Juping Du, Bo Shen, Chunping Li

Connect to this object online.

The IGSF1 Deficiency Syndrome May Present with Normal Free T4 Levels, Severe Obesity, or Premature Testicular Growth by Steven Ghanny, Aliza Zidell, Helio Pedro, Sjoerd D. Joustra, Monique Losekoot, Jan M. Wit, Javier Aisenberg

Connect to this object online.

<i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case by Nikolay N. Murashkin, Roman V. Epishev, Olesya D. Dubenko, Alexander I. Materikin, Leonid A. Opryatin, Roman A. Ivanov, Alena A. Savelova, Maria A. Leonova

Connect to this object online.

Reticulate Acropigmentation Of Kitamura by Pavithran K

Connect to this object online.