Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Muneera Al Husain"'
Autor:
Salma M. Wakil, Fatma Alzahrani, Fahad A. Bashiri, M Al Shammari, W Alamoudi, Stefan T. Arold, Mustafa A. Salih, P El.Fishway, Ranad Shaheen, Abdulaziz Al-Saman, A Ercan Sencicek, Niema Ibrahim, M. Hashem, N Abd El.Meguid, Wafaa Eyaid, Majid Alfadhel, Hessa S. Alsaif, Rehab Ali, Ali H Alwadei, Nada Al-Tassan, Anas M. Alazami, Nour Ewida, Dorota Monies, Amal Y. Kentab, Mohamed Abouelhoda, Matthew W. State, Haifa Alsedairy, Adel A.H. Mahmoud, Zuhair N. Al-Hassnan, A Al Asmari, M Alsughayir, R Osama Khalil, M Alnaser, Amira Masri, Khalid A. Alhasan, Adel F. Hashish, Mohammed M. Saleh, Amal M. Hashem, Hanan E. Shamseldin, Nisha Patel, Eissa Faqeih, Sateesh Maddirevula, Shamsa Anazi, Firdous Abdulwahab, Muneera Al-Husain, Fowzan S. Alkuraya, Tawfeg Ben-Omran, H Al sharif
Publikováno v:
Molecular psychiatry. 22(4)
Intellectual disability (ID) is a measurable phenotypic consequence of genetic and environmental factors. In this study, we prospectively assessed the diagnostic yield of genomic tools (molecular karyotyping, multi-gene panel and exome sequencing) in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98961e3bce4a18608ddc49da0002a817
https://pubmed.ncbi.nlm.nih.gov/27431290
https://pubmed.ncbi.nlm.nih.gov/27431290
Publikováno v:
Clinical Genetics. 80:196-198
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6717ad4185438b88a3668215f221076e
https://doi.org/10.1111/j.1399-0004.2010.01613.x
https://doi.org/10.1111/j.1399-0004.2010.01613.x
Autor:
Muneera Al Husain, Osama K. Zaki
Publikováno v:
Human Heredity. 49:208-214
We reviewed cytogenetic studies that have been done in 1,000 consecutive non-oncology samples that were referred to the Cytogenetics Unit at King Khalid University Hospital, Riyadh, Saudi Arabia. The cases were grouped according to the referral diagn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28d5042834687eb6ea967b07b9c883a5
https://doi.org/10.1159/000022877
https://doi.org/10.1159/000022877
Autor:
Muneera J. Alshammari, Ramil R. Noche, Tarfa Al-Sheddi, Nouran Adly, Hanan E. Shamseldin, Muneera Al-Husain, Mohammed S. Al-Dosari, Fowzan S. Alkuraya, Eissa Faqeih, Asma Sunker, Sean G. Megason, Ranad Shaheen, Futwan Al-Mohanna
Primordial dwarfism (PD) is a phenotype characterized by profound growth retardation that is prenatal in onset. Significant strides have been made in the last few years toward improved understanding of the molecular underpinning of the limited growth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::697f5c0c2df59b38b37282c2151ad9e2
https://europepmc.org/articles/PMC3415549/
https://europepmc.org/articles/PMC3415549/
Publikováno v:
Europe PubMed Central
Studies on fragile X syndrome are scarce in Saudi Arabia and other countries of the Arabian Peninsula. The few studies previously done have either been in the form of case reports or those performed on institutionalized mentally retarded patients. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e7a91c5fe984784b050c2c7cfe2a922
https://pubmed.ncbi.nlm.nih.gov/17322735
https://pubmed.ncbi.nlm.nih.gov/17322735
Autor:
P. J. Patel, Abdullah M. Abo Bakr, Muneera Al Husain, Abdullah S. Al Herbish, Asal I. Al Samarrai, Akram J. Jawad, Abdullah A. Al Rabeah, Mohammed A. Abdullah, Nasir A.M. Al Jurayyan
Publikováno v:
Europe PubMed Central
Sexual ambiguity is a complex and often confusing medical problem. In addition to the life-threatening adrenal crises which may accompany some forms, ambiguity of the genitalia may lead to incorrect sex assignment by parents and/or health personnel.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0758cfd39aff65719e67a3f377a49e38
https://pubmed.ncbi.nlm.nih.gov/17372394
https://pubmed.ncbi.nlm.nih.gov/17372394
Autor:
Taro Yamashita, Yukio Ando, Jurg Ott, Nimai Chandra Saha, Gunhild Beckman, P. Tabatabaie, P.I. Ohlsson, Sung Han Kim, Jerry Halpern, Sook Hwan Lee, Alice S. Whittemore, Sanmay Bandyopadhyay, Muneera Al Husain, Andrew D. Paterson, Aditi Bandyopadhyay, David M.J. Naimark, Sung Soo Hong, Kazuhiro Tashima, Un Kyung Kim, Uma B. Dasgupta, Chung Choo Lee, Ajita Bhat, Sun-Wei Guo, Masaaki Nakamura, Merrill D. Benson, G.F. van Landeghem, Kamran Hamidi Asl, Vaidutis Kučinskas, Simon Heath, Jae Jin Chae, Yukio Kususe, Yong Namkoong, Helena Korpelainen, Osama K. Zaki, Arturas Petronis, Min Soon Cho, Manju Dutta Chowdhury
Publikováno v:
Human Heredity. 49:239-240
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f6ccde61ea3d908d3be6f10cb0ac3a6
https://doi.org/10.1159/000022883
https://doi.org/10.1159/000022883
Autor:
Ajita Bhat, Chung Choo Lee, Masaaki Nakamura, Merrill D. Benson, G.F. van Landeghem, Osama K. Zaki, Arturas Petronis, Simon Heath, Kamran Hamidi Asl, Uma B. Dasgupta, Sanmay Bandyopadhyay, Jae Jin Chae, Yukio Kususe, Yong Namkoong, Alice S. Whittemore, Vaidutis Kučinskas, Yukio Ando, Jurg Ott, Taro Yamashita, Aditi Bandyopadhyay, Muneera Al Husain, Un Kyung Kim, Helena Korpelainen, Sun-Wei Guo, P.I. Ohlsson, Min Soon Cho, Manju Dutta Chowdhury, Sung Han Kim, Nimai Chandra Saha, Gunhild Beckman, P. Tabatabaie, David M.J. Naimark, Kazuhiro Tashima, Jerry Halpern, Andrew D. Paterson, Sung Soo Hong, Sook Hwan Lee
Publikováno v:
Human Heredity. 49:236-236
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::473e12a8f5c3842e043e055aa1ebd513
https://doi.org/10.1159/000022881
https://doi.org/10.1159/000022881
Autor:
Muneera Al-Husain, P. J. Patel
Publikováno v:
Annals of Saudi Medicine. 9:212-213
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07876233694e5f44ca389b3051c8e399
https://doi.org/10.5144/0256-4947.1989.212
https://doi.org/10.5144/0256-4947.1989.212