Consanguinity :: https://phgkb.cdc.gov/GAPPKB/phgHome.do :: Consanguinity

https://phgkb.cdc.gov/GAPPKB/phgHome.do

From HuGE Literature Finder Database

This database contains published literature on genetic associations and other human genome epidemiology

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• Associations of recurrent miscarriages with chromosomal abnormalities, thrombophilia allelic polymorphisms and/or consanguinity in Saudi Arabia.  
  BMC medical genetics 2016 Oct 17 (Suppl 1): 69.
  Turki Rola F, Assidi Mourad, Banni Huda A, Zahed Hanan A, Karim Sajjad, Schulten Hans-Juergen, Abu-Elmagd Muhammad, Rouzi Abdulrahim A, Bajouh Osama, Jamal Hassan S, Al-Qahtani Mohammed H, Abuzenadah Adel
• Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa Syndrome.  
  American journal of human genetics 2016 Sep .
  Zhu Fuxi, Wang Fengsong, Yang Xiaoyu, Zhang Jingjing, Wu Huan, Zhang Zhou, Zhang Zhiguo, He Xiaojin, Zhou Ping, Wei Zhaolian, Gecz Jozef, Cao Yunx
• Pediatric thromboembolism: a national survey in Japan.  
  International journal of hematology 2016 Aug .
  Ishiguro Akira, Ezinne Chibueze Chioma, Michihata Nobuaki, Nakadate Hisaya, Manabe Atsushi, Taki Masashi, Shima Mido
• Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield.  
  Molecular psychiatry 2016 Jul .
  Anazi S, Maddirevula S, Faqeih E, Alsedairy H, Alzahrani F, Shamseldin H E, Patel N, Hashem M, Ibrahim N, Abdulwahab F, Ewida N, Alsaif H S, Al Sharif H, Alamoudi W, Kentab A, Bashiri F A, Alnaser M, AlWadei A H, Alfadhel M, Eyaid W, Hashem A, Al Asmari A, Saleh M M, AlSaman A, Alhasan K A, Alsughayir M, Al Shammari M, Mahmoud A, Al-Hassnan Z N, Al-Husain M, Osama Khalil R, Abd El Meguid N, Masri A, Ali R, Ben-Omran T, El Fishway P, Hashish A, Ercan Sencicek A, State M, Alazami A M, Salih M A, Altassan N, Arold S T, Abouelhoda M, Wakil S M, Monies D, Shaheen R, Alkuraya F
• Homozygosity mapping guided next generation sequencing to identify the causative genetic variation in inherited retinal degenerative diseases.  
  Journal of human genetics 2016 Jul .
  Sundaramurthy Srilekha, Swaminathan Meenakshi, Sen Parveen, Arokiasamy Tharigopala, Deshpande Swati, John Neetha, Gadkari Rupali A, Mannan Ashraf U, Soumittra Nagasa

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