Results 211 to 220 of about 3,113,716 (239)

Inherited bone marrow failure with ERCC6L2 gene mutation: presentation of aplastic anemia in a 3-year-old child: a case report. [PDF]

J Med Case Rep
Mengistu AG, Heyi YS, Temesgen NE, Aweke SK, Assale NM, Tsega HM, Merahi MK.   +6 more
europepmc   +1 more source

The Edification of Manuela Xiqués: Slavery, Finance, Biography, and the Construction of Modern Barcelona

Gender &History, EarlyView.
ABSTRACT An analysis of the dual biographies, economic and domestic, of Manuela Xiqués, an enslaver from nineteenth‐century Cuba and Spain, deepens our understanding of the role of European and Creole women in the nineteenth‐century Atlantic. This essay foregrounds the role of literature, namely family biography, as a locus of the processes of ...
Lisa Surwillo, Martín Rodrigo Alharilla
wiley   +1 more source

Nonsyndromic Hypodontia Including Bilateral Agenesis of Permanent Maxillary Canines: A Case Report. [PDF]

Case Rep Dent
Kurosaka A, Saijo H.
europepmc   +1 more source

Accommodating Women: Geographies of Citizenship in the Twentieth‐Century Campaign for Women's Jury Rights

Gender &History, EarlyView.
ABSTRACT Australian women were among the first in the world to receive electoral suffrage, yet it took until 1997 before they had full equality of jury suffrage. This article examines the debate around female jurors by focusing less on discourses of citizenship than on the subterranean spatial arrangements upon which equality depended.
Alecia Simmonds
wiley   +1 more source

A Novel <i>MPIG6B</i> Gene Variant Identified in a Patient with Congenital Thrombocytopenia from Türkiye [PDF]

Turk J Haematol
Kılınç Oktay B, Durmaz B, Çınar Özel S, Ocak S, Tiraje Celkan T.   +4 more
europepmc   +1 more source

Fetal rights from Islamic and contemporary legal perspectives: a scoping review. [PDF]

Reprod Health
Kakrodi SP, Sighaldeh SS, Mosadeghrad MA, Abbassi M.   +3 more
europepmc   +1 more source

Structural, economic, and socio-cultural barriers to birth and death registration in Iran: a qualitative study. [PDF]

Int J Equity Health
Asadisarvestani K.
europepmc   +1 more source

Beyond the genome: clinical challenges in diagnosing <i>LONP1</i>-related mitochondrial disorders. [PDF]

Front Cell Dev Biol
Jiang Q, Duan J, Liu C, Zhu Y, Zeng Q, Hu Y, Luo Z, Cao D, Liao J, Chen L.   +9 more
europepmc   +1 more source

Pearson syndrome: expanding the clinical spectrum of a mitochondrial cytopathy-a case report. [PDF]

J Med Case Rep
Faisal A, Waqas H, Masood H, Butt A, Rahman S, Hameed MS, Zaidi SRH, Iqbal A, Naveed MU.   +8 more
europepmc   +1 more source

Diagnostic yield and variant spectrum of whole-exome sequencing in Iranian probands with congenital and early-onset ocular disorders. [PDF]

Mol Genet Metab Rep
Asadi A, Sadat Shandiz SA, Ebrahimi A, Hosseini ZS, Shirsalimi N, Neamatzadeh H, Ebrahimi A.   +6 more
europepmc   +1 more source