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Correction: Correlating SFTPC gene variants to interstitial lung disease in Egyptian children.

Autor: Abdel Megeid AK; Pediatric Department, Cairo University, Giza, Egypt., Refeat MM; Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt., Ashaat EA; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt., El-Kamah G; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt., El-Saiedi SA; Pediatric Department, Cairo University, Giza, Egypt., Elfalaki MM; Pediatric Department, Cairo University, Giza, Egypt., El Ruby MO; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt., Amr KS; Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt. khalda_nrc@yahoo.com.

Publikováno v: Journal, genetic engineering & biotechnology [J Genet Eng Biotechnol] 2022 Sep 21; Vol. 20 (1), pp. 137. Date of Electronic Publication: 2022 Sep 21.

Correlating SFTPC gene variants to interstitial lung disease in Egyptian children.

Autor: Abdel Megeid AK; Pediatric Department, Cairo University, Giza, Egypt., Refeat MM; Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt., Ashaat EA; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt., El-Kamah G; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt., El-Saiedi SA; Pediatric Department, Cairo University, Giza, Egypt., Elfalaki MM; Pediatric Department, Cairo University, Giza, Egypt., El Ruby MO; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt., Amr KS; Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt. khalda_nrc@yahoo.com.

Publikováno v: Journal, genetic engineering & biotechnology [J Genet Eng Biotechnol] 2022 Aug 08; Vol. 20 (1), pp. 117. Date of Electronic Publication: 2022 Aug 08.

Clinical and genetic characterization of ten Egyptian patients with Wolf-Hirschhorn syndrome and review of literature.

Autor: Mekkawy MK; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., Kamel AK; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., Thomas MM; Clinical Genetics Department, National Research Centre, Cairo, Egypt., Ashaat EA; Clinical Genetics Department, National Research Centre, Cairo, Egypt., Zaki MS; Clinical Genetics Department, National Research Centre, Cairo, Egypt., Eid OM; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., Ismail S; Clinical Genetics Department, National Research Centre, Cairo, Egypt., Hammad SA; Clinical Genetics Department, National Research Centre, Cairo, Egypt., Megahed H; Clinical Genetics Department, National Research Centre, Cairo, Egypt., ElAwady H; Pediatric Department, Faculty of Medicine, Fayoum unIversity, Fayoum, Egypt., Refaat KM; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., Hussien S; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., Helmy N; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., Abd Allah SG; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., Mohamed AM; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., El Ruby MO; Clinical Genetics Department, National Research Centre, Cairo, Egypt.

Publikováno v: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2021 Feb; Vol. 9 (2), pp. e1546. Date of Electronic Publication: 2020 Nov 20.

Rubinstein-Taybi syndrome in diverse populations.

Autor: Tekendo-Ngongang C; Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland, USA., Owosela B; Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland, USA., Fleischer N; FDNA Inc., Boston, Massachusetts, USA., Addissie YA; Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland, USA., Malonga B; Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland, USA., Badoe E; Department of Child Health, School of Medicine and Dentistry, College of Health Sciences, Accra, Ghana., Gupta N; Division of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India., Moresco A; Servicio de Genética, Hospital de Pediatría Garrahan, Buenos Aires, Argentina., Huckstadt V; Servicio de Genética, Hospital de Pediatría Garrahan, Buenos Aires, Argentina., Ashaat EA; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt., Hussen DF; Cytogenetic Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt., Luk HM; Department of Health, Clinical Genetic Service, Hong Kong Special Administrative Region, Hong Kong, China., Lo IFM; Department of Health, Clinical Genetic Service, Hong Kong Special Administrative Region, Hong Kong, China., Hon-Yin Chung B; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China., Fung JLF; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China., Moretti-Ferreira D; Department of Genetics, Institute of Biosciences, Sao Paulo State University-UNESP, Botucatu, São Paulo, Brazil., Batista LC; Department of Genetics, Institute of Biosciences, Sao Paulo State University-UNESP, Botucatu, São Paulo, Brazil., Lotz-Esquivel S; Rare and Orphan Disease Multidisciplinary Clinic, Hospital San Juan de Dios (CCSS), San José, Costa Rica., Saborio-Rocafort M; Medical Genetics and Metabolism Department, National Children's Hospital 'Dr. Carlos Sáenz Herrera' (CCSS), San José, Costa Rica., Badilla-Porras R; Medical Genetics and Metabolism Department, National Children's Hospital 'Dr. Carlos Sáenz Herrera' (CCSS), San José, Costa Rica., Penon Portmann M; Medical Genetics and Metabolism Department, National Children's Hospital 'Dr. Carlos Sáenz Herrera' (CCSS), San José, Costa Rica.; Division of Medical Genetics, Department of Pediatrics & Institute for Human Genetics, University of California San Francisco, San Francisco, California, USA., Jones KL; Division of Medical Genetics and Metabolism, Children's Hospital of The King's Daughters, Norfolk, Virginia, USA., Abdul-Rahman OA; Munroe-Meyer institute for Genetics and Rehabilitation, University of Nebraska Medical Center, Omaha, Nebraska, USA., Uwineza A; Centre for Human Genetics, School of Medicine and Pharmacy, College of Medicine and Health Sciences, University of Rwanda, Kigali, Rwanda., Prijoles EJ; Greenwood Genetic Center, Greenwood, South Carolina, USA., Ifeorah IK; Nigerian Air Force Hospital, Nigerian Air Force, Abuja, Nigeria., Llamos Paneque A; Medical Genetics Service, Specialty Hospital of the Armed Forces No. 1, International University of Ecuador, Sciences of Life Faculty, School of Dentistry, Quito, Ecuador., Sirisena ND; Human Genetics Unit, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka., Dowsett L; Kapi'olani Medical Center and University of Hawai'i, Honolulu, Hawaii, USA., Lee S; Kapi'olani Medical Center and University of Hawai'i, Honolulu, Hawaii, USA., Cappuccio G; Department of Translational Medicine, Section of Pediatrics, Federico II University, Naples, Italy.; Telethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy., Kitchin CS; Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa., Diaz-Kuan A; Instituto de Medicina Genética, Santiago de Surco, Lima, Peru., Thong MK; Department of Paediatrics, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia., Obregon MG; Servicio de Genética, Hospital de Pediatría Garrahan, Buenos Aires, Argentina., Mutesa L; Centre for Human Genetics, School of Medicine and Pharmacy, College of Medicine and Health Sciences, University of Rwanda, Kigali, Rwanda., Dissanayake VHW; Human Genetics Unit, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka., El Ruby MO; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt., Brunetti-Pierri N; Department of Translational Medicine, Section of Pediatrics, Federico II University, Naples, Italy.; Telethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy., Ekure EN; Department of Paediatrics, College of Medicine, University of Lagos, Lagos, Nigeria., Stevenson RE; Greenwood Genetic Center, Greenwood, South Carolina, USA., Muenke M; Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland, USA., Kruszka P; Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland, USA.

Publikováno v: American journal of medical genetics. Part A [Am J Med Genet A] 2020 Dec; Vol. 182 (12), pp. 2939-2950. Date of Electronic Publication: 2020 Sep 27.