Results 121 to 130 of about 21,992 (163)

A Case of Congenital Central Hypothyroidism Caused by a Novel Variant (Gln1255Ter) in IGSF1 Gene [PDF]

open access: yesJ Clin Res Pediatr Endocrinol, 2021
Türkkahraman D   +3 more
europepmc   +1 more source

Determination of the relationship between major histocompatibility complex alleles and childhood onset obsessive-compulsive disorder. [PDF]

open access: yesTurk J Med Sci, 2022
Lüleyap Ü   +9 more
europepmc   +1 more source

Comparison of maternal serum NRG-4 levels in healthy and preeclamptic pregnancies [PDF]

open access: yesJ Turk Ger Gynecol Assoc, 2022
Yakut K   +5 more
europepmc   +1 more source

Serum Ghrelin and Glucagon-like Peptide 1 Levels in Children with Prader-Willi and Bardet-Biedl Syndromes [PDF]

open access: yesJ Clin Res Pediatr Endocrinol
Türkkahraman D   +3 more
europepmc   +1 more source

A Boy with 46,XX Karyotype (SRY Double-positive) and a Leydig Cell Tumor [PDF]

open access: yesJ Clin Res Pediatr Endocrinol
Güllü M   +4 more
europepmc   +1 more source

The Manchester procedure combined with laparoscopic sacrohysteropexy by retroperitoneal tunneling [PDF]

open access: yesJ Turk Ger Gynecol Assoc, 2022
Seçkin KD   +4 more
europepmc   +1 more source

Organik ürünler doğal mı? değil mi? [PDF]

open access: yes, 2011
Cetiner, Selim, Çetiner, Selim
core  

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