Works matching IS 14712350 AND DT 2020 AND VI 21

Results: 242

A novel genetic variant in DNAI2 detected by custom gene panel in a newborn with Primary Ciliary Dyskinesia: case report.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01160-5

By:

Rocca, Maria Santa;
Piatti, Gioia;
Michelucci, Angela;
Guazzo, Raffaella;
Bertini, Veronica;
Vinanzi, Cinzia;
Caligo, Maria Adelaide;
Valetto, Angelo;
Foresta, Carlo

Publication type:

Article

Hypoglycemia and Dandy-Walker variant in a Kabuki syndrome patient: a case report.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01117-8

By:

Guo, Wei;
Zhao, Yanguo;
Li, Shuwei;
Wang, Jingqun;
Liu, Xiang

Publication type:

Article

Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01168-x

By:

Khatami, Somayeh;
Askari, Masomeh;
Bahreini, Fatemeh;
Hashemzadeh-Chaleshtori, Morteza;
Hematian, Saeed;
Asgharzade, Samira

Publication type:

Article

Interleukin-4 gene polymorphism (C33T) and the risk of the asthma: a meta-analysis based on 24 publications.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01169-w

By:

Imani, Danyal;
Eslami, Mohammad Masoud;
Anani-Sarab, Gholamreza;
Aliyu, Mansur;
Razi, Bahman;
Rezaei, Ramazan

Publication type:

Article

Incidence of Huntington disease in a northeastern Spanish region: a 13-year retrospective study at tertiary care centre.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01174-z

By:

Sienes Bailo, Paula;
Lahoz, Raquel;
Sánchez Marín, Juan Pelegrín;
Izquierdo Álvarez, Silvia

Publication type:

Article

A non-synonymous variant rs12614 of complement factor B associated with risk of chronic hepatitis B in a Korean population.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01177-w

By:

Seo, Jung Yeon;
Shin, Joong-Gon;
Youn, Byeong Ju;
Namgoong, Suhg;
Cheong, Hyun Sub;
Kim, Lyoung Hyo;
Kim, Ji On;
Shin, Hyoung Doo;
Kim, Yoon Jun

Publication type:

Article

Application of next generation sequencing in genetic counseling a case of a couple at risk of cystinosis.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01167-y

By:

Ouhenach, Mouna;
Zrhidri, Abdelali;
Jaouad, Imane Cherkaoui;
Smaili, Wiam;
Sefiani, Abdelaziz

Publication type:

Article

DGAT1 mutations leading to delayed chronic diarrhoea: a case report.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01164-1

By:

Xu, Luojia;
Gu, Weizhong;
Luo, Youyou;
Lou, Jingan;
Chen, Jie

Publication type:

Article

Case report: progressive familial intrahepatic cholestasis type 3 with compound heterozygous ABCB4 variants diagnosed 15 years after liver transplantation.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01173-0

By:

Goubran, Mariam;
Aderibigbe, Ayodeji;
Jacquemin, Emmanuel;
Guettier, Catherine;
Girgis, Safwat;
Bain, Vincent;
Mason, Andrew L.

Publication type:

Article

Two novel mutations in the DNAH11 gene in primary ciliary dyskinesia (CILD7) with considerable variety in the clinical and beating cilia phenotype.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01171-2

By:

Schultz, Rüdiger;
Elenius, Varpu;
Lukkarinen, Heikki;
Saarela, Tanja

Publication type:

Article

First submicroscopic inversion of the OPA1 gene identified in dominant optic atrophy – a case report.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01166-z

By:

Weisschuh, Nicole;
Mazzola, Pascale;
Heinrich, Tilman;
Haack, Tobias;
Wissinger, Bernd;
Tonagel, Felix;
Kelbsch, Carina

Publication type:

Article

First case report of cerebral folate deficiency caused by a novel mutation of FOLR1 gene in a Chinese patient.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01162-3

By:

Zhang, Ciliu;
Deng, Xiaolu;
Wen, Yafei;
He, Fang;
Yin, Fei;
Peng, Jing

Publication type:

Article

Mice lacking global Stap1 expression do not manifest hypercholesterolemia.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01176-x

By:

Kanuri, Babunageswararao;
Fong, Vincent;
Haller, April;
Hui, David Y.;
Patel, Shailendra B.

Publication type:

Article

Genome-wide association study of prevalent and persistent cervical high-risk human papillomavirus (HPV) infection.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01156-1

By:

Adebamowo, Sally N.;
Adeyemo, Adebowale A.;
Rotimi, Charles N.;
Olaniyan, Olayinka;
Offiong, Richard;
Adebamowo, Clement A.;
for the H3Africa ACCME Research Group;
Odutola, Michael;
Dareng, Eileen O.;
Famooto, Ayotunde O.;
Adebiyi, Ruxton

Publication type:

Article

Next generation sequencing of RB1gene for the molecular diagnosis of ethnic minority with retinoblastoma in Yunnan.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01150-7

By:

Zhang, Zhen;
Xiao, Yi-shuang;
Shen, Ru;
Jiang, Hong-chao;
Tan, Li;
Li, Ren-qiu;
Yang, Xiao-hong;
Gu, Huai-yu;
He, Wen-Ji;
Ma, Jing

Publication type:

Article

Overwhelming sepsis in a neonate affected by Zellweger syndrome due to a compound heterozygosis in PEX 6 gene: a case report.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01175-y

By:

Lucaccioni, Laura;
Righi, Beatrice;
Cingolani, Greta Miriam;
Lugli, Licia;
Della Casa, Elisa;
Torcetta, Francesco;
Iughetti, Lorenzo;
Berardi, Alberto

Publication type:

Article

Wilson disease, ABCC2 c.3972C > T polymorphism and primary liver cancers: suggestions from a familial cluster.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01165-0

By:

Brandi, Giovanni;
Rizzo, Alessandro;
Deserti, Marzia;
Relli, Valeria;
Indio, Valentina;
Bin, Sofia;
Pariali, Milena;
Palloni, Andrea;
De Lorenzo, Stefania;
Tovoli, Francesco;
Tavolari, Simona

Publication type:

Article

Congenital thrombocytopenia associated with GNE mutations in twin sisters: a case report and literature review.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01163-2

By:

Li, Xin;
Li, Ying;
Lei, Min;
Tian, Jing;
Yang, Zuocheng;
Kuang, Shoujin;
Tan, Yanjuan;
Bo, Tao

Publication type:

Article

Mediation by differential DNA methylation of known associations between single nucleotide polymorphisms and bladder cancer risk.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01172-1

By:

Jordahl, Kristina M.;
Phipps, Amanda I.;
Randolph, Timothy W.;
Tinker, Lesley F.;
Nassir, Rami;
Hou, Lifang;
Anderson, Garnet L.;
Kelsey, Karl T.;
White, Emily;
Bhatti, Parveen

Publication type:

Article

Characterization of an N-terminal Na<sub>v</sub>1.5 channel variant – a potential risk factor for arrhythmias and sudden death?

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01170-3

By:

Scheiper-Welling, Stefanie;
Zuccolini, Paolo;
Rauh, Oliver;
Beckmann, Britt-Maria;
Geisen, Christof;
Moroni, Anna;
Thiel, Gerhard;
Kauferstein, Silke

Publication type:

Article

Novel nonsense mutation p. Gln264Ter in the ANK1 confirms causative role for hereditary spherocytosis: a case report.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01161-4

By:

Chai, Senmao;
Jiao, Rong;
Sun, Xiaodong;
Fu, Pan;
Zhao, Qiang;
Sang, Ming

Publication type:

Article

Novel compound heterozygous TARS2 variants in a Chinese family with mitochondrial encephalomyopathy: a case report.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01149-0

By:

Li, Xiaojing;
Peng, Bingwei;
Hou, Chi;
Li, Jinliang;
Zeng, Yiru;
Wu, Wenxiao;
Liao, Yinting;
Tian, Yang;
Chen, Wen-Xiong

Publication type:

Article

Deep vein thrombosis inhibitor may play a therapeutic role in post-stroke patients.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01108-9

By:

Xiang, Xixi;
Yuan, Di;
Kong, Peiyan;
Chen, Ting;
Yao, Han;
Lin, Shijia;
Zhang, Xi;
Cao, Hongbao

Publication type:

Article

The association between genetic polymorphisms in ABCG2 and SLC2A9 and urate: an updated systematic review and meta-analysis.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01147-2

By:

Lukkunaprasit, Thitiya;
Rattanasiri, Sasivimol;
Turongkaravee, Saowalak;
Suvannang, Naravut;
Ingsathit, Atiporn;
Attia, John;
Thakkinstian, Ammarin

Publication type:

Article

Prenatal diagnosis of Duchenne muscular dystrophy revealed a novel mosaic mutation in Dystrophin gene: a case report.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01157-0

By:

Wang, Yan;
Chen, Yuhan;
Wang, San Mei;
Liu, Xin;
Gu, Ya Nan;
Feng, Zhichun

Publication type:

Article

Hereditary intrinsic factor deficiency in China caused by a novel mutation in the intrinsic factor gene—a case report.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01158-z

By:

Ruan, Jing;
Han, Bing;
Zhuang, Junling;
Chen, Miao;
Chen, Fangfei;
Huang, Yuzhou;
Zhou, Wenzhe

Publication type:

Article

Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn's disease subjects.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01115-w

By:

Turpin, Williams;
Bedrani, Larbi;
Espin-Garcia, Osvaldo;
Xu, Wei;
Silverberg, Mark S.;
Smith, Michelle I.;
Garay, Juan Antonio Raygoza;
Lee, Sun-Ho;
Guttman, David S.;
Griffiths, Anne;
Moayyedi, Paul;
Panaccione, Remo;
Huynh, Hien;
Steinhart, Hillary A.;
Aumais, Guy;
Dieleman, Levinus A.;
Turner, Dan;
CCC IBD GEM Project research team;
Abreu, Maria;
Beck, Paul

Publication type:

Article

Novel loss-of-function variants in TRIO are associated with neurodevelopmental disorder: case report.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01159-y

By:

Schultz-Rogers, Laura;
Muthusamy, Karthik;
Pinto e Vairo, Filippo;
Klee, Eric W.;
Lanpher, Brendan

Publication type:

Article

The role of UGT1A1 (c.-3279 T > G) gene polymorphisms in neonatal hyperbilirubinemia susceptibility.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01155-2

By:

Li, Zijin;
Song, Li;
Hao, Lihong

Publication type:

Article

Two novel PCDH19 mutations in Russian patients with epilepsy with intellectual disability limited to females: a case report.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01119-6

By:

Kozina, Anastasiya Aleksandrovna;
Okuneva, Elena Grigorievna;
Baryshnikova, Natalia Vladimirovna;
Fedonyuk, Inessa Dmitrievna;
Kholin, Alexey Aleksandrovich;
Il'ina, Elena Stepanovna;
Krasnenko, Anna Yurievna;
Stetsenko, Ivan Fedorovich;
Plotnikov, Nikolay Alekseevich;
Klimchuk, Olesia Igorevna;
Surkova, Ekaterina Ivanovna;
Ilinsky, Valery Vladimirovich

Publication type:

Article

NGS-based expanded carrier screening for genetic disorders in North Indian population reveals unexpected results – a pilot study.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01153-4

By:

Singh, Kanika;
Bijarnia-Mahay, Sunita;
Ramprasad, V. L.;
Puri, Ratna Dua;
Nair, Sandhya;
Sharda, Sheetal;
Saxena, Renu;
Kohli, Sudha;
Kulshreshtha, Samarth;
Ganguli, Indrani;
Gujral, Kanwal;
Verma, Ishwar C.

Publication type:

Article

The first case report of Kyphoscoliotic Ehlers-Danlos syndrome of chinese origin with a novel PLOD1 gene mutation.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01154-3

By:

Ni, Xiaolin;
Jin, Chenxi;
Jiang, Yan;
Wang, Ou;
Li, Mei;
Xing, Xiaoping;
Xia, Weibo

Publication type:

Article

Novel variants of ABCA4 in Han Chinese families with Stargardt disease.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01152-5

By:

Hu, Fang-Yuan;
Gao, Feng-Juan;
Li, Jian-kang;
Xu, Ping;
Wang, Dan-Dan;
Zhang, Sheng-Hai;
Wu, Ji-Hong

Publication type:

Article

A novel PIK3R1 mutation of SHORT syndrome in a Chinese female with diffuse thyroid disease: a case report and review of literature.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01146-3

By:

Sun, Liying;
Zhang, Qianwen;
Li, Qun;
Tang, Yijun;
Wang, Yirou;
Li, Xin;
Li, Niu;
Wang, Jian;
Wang, Xiumin

Publication type:

Article

Genetic polymorphisms of PGF and TNFAIP2 genes related to cervical cancer risk among Uygur females from China.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01144-5

By:

Ainiwaer, Zumurelaiti;
Maisaidi, Reyilanmu;
Liu, Jing;
Han, Lili;
Husaiyin, Sulaiya;
Lu, Jing;
Niyazi, Mayinuer

Publication type:

Article

Recessive myotonia congenita caused by a homozygous splice site variant in CLCN1 gene: a case report.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01128-5

By:

Sparber, Peter;
Sharova, Margarita;
Filatova, Alexandra;
Shchagina, Olga;
Ivanova, Evgeniya;
Dadali, Elena;
Skoblov, Mikhail

Publication type:

Article

Medical genetics studies at the SBB-2019 and MGNGS-2019 conferences.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01109-8

By:

Baranova, Ancha V.;
Leberfarb, Elena Yu.;
Lebedev, Georgy S.;
Orlov, Yuriy L.

Publication type:

Article

Unannotated single nucleotide polymorphisms in the TATA box of erythropoiesis genes show in vitro positive involvements in cognitive and mental disorders.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01106-x

By:

Ponomarenko, Mikhail;
Sharypova, Ekaterina;
Drachkova, Irina;
Chadaeva, Irina;
Arkova, Olga;
Podkolodnaya, Olga;
Ponomarenko, Petr;
Kolchanov, Nikolay;
Savinkova, Ludmila

Publication type:

Article

Genetic polymorphisms of PIP5K2A and course of schizophrenia.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01107-w

By:

Poltavskaya, Evgeniya G.;
Fedorenko, Olga Yu.;
Vyalova, Natalya M.;
Kornetova, Elena G.;
Bokhan, Nikolay A.;
Loonen, Anton J. M.;
Ivanova, Svetlana A.

Publication type:

Article

p.Arg72Pro polymorphism of P53 and breast cancer risk: a meta-analysis of case-control studies.

Published in:

2020

By:

Diakite, Brehima;
Kassogue, Yaya;
Dolo, Guimogo;
Wang, Jun;
Neuschler, Erin;
Kassogue, Oumar;
Keita, Mamadou L;
Traore, Cheick B;
Kamate, Bakarou;
Dembele, Etienne;
Nadifi, Sellama;
Murphy, Robert L;
Doumbia, Seydou;
Hou, Lifang;
Maiga, Mamoudou

Publication type:

Literature Review

Understanding the molecular association between hyperkalemia and lung squamous cell carcinomas.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01099-7

By:

Meng, Xianping;
Lu, Hongyan;
Jiang, Xia;
Huang, Bin;
Wu, Song;
Yu, Guiping;
Cao, Hongbao

Publication type:

Article

Prenatal diagnosis of Norrie disease after whole exome sequencing of an affected proband during an ongoing pregnancy: a case report.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01093-z

By:

Marakhonov, Andrey V.;
Mishina, Irina A.;
Kadyshev, Vitaly V.;
Repina, Svetlana A.;
Shurygina, Maria F.;
Shchagina, Olga A.;
Vasserman, Natalya N.;
Vasilyeva, Tatyana A.;
Kutsev, Sergey I.;
Zinchenko, Rena A.

Publication type:

Article

A nonsense variant in FBN1 caused autosomal dominant Marfan syndrome in a Chinese family: a case report.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01148-1

By:

Niu, Yuping;
Huang, Sexin;
Wang, Zeyu;
Xu, Peiwen;
Wang, Lijuan;
Li, Jie;
Gao, Ming;
Gao, Xuan;
Gao, Yuan

Publication type:

Article

Effect of DNMT3A polymorphisms on CpG island hypermethylation in gastric mucosa.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01142-7

By:

Takano, Hikaru;
Shibata, Tomoyuki;
Nakamura, Masakatsu;
Sakurai, Naoko;
Hayashi, Tasuku;
Ota, Masafumi;
Nomura-Horita, Tomoe;
Hayashi, Ranji;
Shimasaki, Takeo;
Otsuka, Toshimi;
Tahara, Tomomitsu;
Arisawa, Tomiyasu

Publication type:

Article

Investigation of INDEL variants in apoptosis: the relevance to gastric cancer.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01138-3

By:

Cavalcante, Giovanna Chaves;
de Moraes, Milene Raiol;
Valente, Cristina Maria Duarte;
Silva, Caio Santos;
Modesto, Antônio André Conde;
de Assumpção, Paula Baraúna;
de Assumpção, Paulo Pimentel;
Santos, Sidney;
Ribeiro-dos-Santos, Ândrea

Publication type:

Article

Development of an immunogenomic landscape for the competing endogenous RNAs network of peri-implantitis.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01145-4

By:

Li, Yang;
Zheng, Jina;
Gong, Chanjuan;
Lan, Kengfu;
Shen, Yuqing;
Ding, Xiaojun

Publication type:

Article

Peritoneal dialysis in an adult patient with tetralogy of Fallot diagnosed with incomplete Alagille syndrome.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01134-7

By:

Ponikowska, Malgorzata;
Pollak, Agnieszka;
Kotwica-Strzalek, Ewa;
Brodowska-Kania, Dorota;
Mosakowska, Magdalena;
Ploski, Rafal;
Niemczyk, Stanislaw

Publication type:

Article

Novel FHL1 mutation variant identified in a patient with nonobstructive hypertrophic cardiomyopathy and myopathy – a case report.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01131-w

By:

Giucă, Adrian;
Mitu, Cristina;
Popescu, Bogdan Ovidiu;
Bastian, Alexandra Eugenia;
Capşa, Răzvan;
Mursă, Adriana;
Rădoi, Viorica;
Popescu, Bogdan Alexandru;
Jurcuţ, Ruxandra

Publication type:

Article

Identification of two novel pathogenic variants of PIBF1 by whole exome sequencing in a 2-year-old boy with Joubert syndrome.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01130-x

By:

Shen, Yue;
Wang, Hao;
Liu, Zhimin;
Luo, Minna;
Ma, Siyu;
Lu, Chao;
Cao, Zongfu;
Yu, Yufei;
Cai, Ruikun;
Chen, Cuixia;
Li, Qian;
Gao, Huafang;
Peng, Yun;
Xu, Baoping;
Ma, Xu

Publication type:

Article

Genotype-phenotype correlation of HbH disease in northern Iraq.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01141-8

By:

Shamoon, Rawand P.;
Yassin, Ahmed K.;
Polus, Ranan K.;
Ali, Mohamad D.

Publication type:

Article