Coinheritance of a Novel Mutation on the HBA1 Gene: c.187delG (p.W62fsX66) [codon 62 (–G) (α1)] with the α212 Patchwork Allele and Hb S [β6(A3)Glu→Val, GAG>GTG; HBB: c.20A>T]

By Scheps Karen G.   De Paula Silvia M.   Bitsman Alicia R.   Freigeiro Daniel H.   Basack F. Nora   Pennesi Sandra P.   Varela Viviana  

Hemoglobin, Vol. 37, Iss. 5, 2013-10 ,pp. : 492-500

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Hb Papanui [α99(G8)Lys→Arg; HBA2: c.299A>G]: A Novel Silent Substitution Interfering in Hb A_1c Determination

By Brennan Stephen O.   Chan Tim  

Hemoglobin, Vol. 37, Iss. 6, 2013-12 ,pp. : 589-592

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Hb Fulton-Georgia [α20(B1)His→Pro; HBA1: c.62A>C]: A New α-Globin Variant Coinherited with α-Thalassemia-2 (3.7 kb deletion) and Hb SC Disease

By Zhuang Lina   Patel Niren   Bryant Shanequa   Kutlar Abdullah   Kutlar Ferdane   Young Andrew N.  

Hemoglobin, Vol. 37, Iss. 5, 2013-10 ,pp. : 481-485

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Association study of the TNF-α −1031T/C and VEGF + 450G/C polymorphisms with susceptibility to endometriosis

By Saliminejad Kioomars   Memariani Toktam   Ardekani Ali M.   Kamali Koorosh   Edalatkhah Haleh   Pahlevanzadeh Zhamak   Khorram Khorshid Hamid Reza  

Gynecological Endocrinology, Vol. 29, Iss. 11, 2013-11 ,pp. : 974-977

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Two Complex Associations of an HBD Mutation and a Rare α Hemoglobinopathy

By Joly Philippe   Lacan Philippe   Garcia Caroline   Francina Alain  

Hemoglobin, Vol. 37, Iss. 5, 2013-10 ,pp. : 486-491

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