• 3-Year-old phenotypic female with campomelic dysplasia and bilateral gonadoblastoma
• A 66-Year-Old Woman with Achondroplasia and Quadriparesis with an Ovarian Cyst Erroneously Diagnosed as Urinary Retention by an Automated Bladder Scan
• A case of dwarfism with total ovarian insufficiency and hyper-secretion of gonadotropic hormone (Turner's syndrome)
• A neonatal ovarian cyst associated with transient endocrine anomalies
• A stone was lifted from her heart: pericardial constriction in 28-year-old patient with Mulibrey nanism
• Altered state of primordial follicles in neonatal and early infantile rats due to maternal hypothyroidism: Light and electron microscopy approach
• Apoptosis of granulosa cells and female infertility in achondroplastic mice expressing mutant fibroblast growth factor receptor 3G374R
• Association of Van Wyk Grumbach and Debre Semelaigne Syndromes with Severe Hypothyroidism
• Bi-allelic recessive loss-of-function mutations in FIGLA cause premature ovarian insufficiency with short stature
• Blepharophimosis Ptosis Epicanthus Inversus Syndrome With Congenital Hypothyroidism and Brachydactyly in a 7-Year-Old Girl
• Cancer in Ecuadorian subjects with Laron syndrome (ELS)
• Case of ovarian agenesis without nanism & with normal feminine morphology
• Case of ovarian agenesis without nanism & with normal feminine morphology
• Chorionic growth hormone-prolactin (CGP): secretion, disposition, biologic activity in man, and postulated function as the "growth hormone" of the 2d half of pregnancy
• Climacteric in untreated isolated growth hormone deficiency
• Clinical effects of pulsatile LH-RH administration on ovulation induction for women with various type of amenorrhea
• Clinical experience with hypothalamic releasing hormones. 1. Thyrotropin-releasing hormone
• Co-existence of infantilism, ovarian agenesis, and reno-pyelo-ureteral abnormalities: pathogenesis of Turner's syndrome and renal nanism
• Concurrent occurrence of chronic lymphocytic thyroiditis with hypothyroidism and growth hormone deficiency in a Turner's syndrome patient
• Congenital hypothyroid female pax8-deficient mice are infertile despite thyroid hormone replacement therapy
• Congenital hypothyroidism with multiple ovarian cysts
• Cretinism with ovarian cyst causing precocious puberty
• CSB-PGBD3 Mutations Cause Premature Ovarian Failure
• Del (X)(p21.2) in a mother and two daughters with variable ovarian function
• Dwarfism caused by ovarian insufficiency
• Embryonic and postnatal development in experimental tryptophan deprived rats. A preliminary study
• Exposure of Pregnant Mice to Perfluorobutanesulfonate Causes Hypothyroxinemia and Developmental Abnormalities in Female Offspring
• Expression of XPG protein in human normal and tumor tissues
• Failure of sexual maturation in Mulibrey nanism
• FGFR signalling in women's cancers
• First report on the isolation of Chlamydia abortus from female dromedary camels with ovarian hydrobursitis
• FSH, LH and prolactin levels, ovarian follicular development and ovarian responsiveness to FSH in the Snell dwarf mouse
• Giant ovarian cyst in a dwarf
• Gonadal dysgenesis
• Growth hormone treatment inTurner syndrome: data and reflections
• Growth hormone treatment of patients with Fanconi anemia after hematopoietic cell transplantation
• Gynecological tumors in Mulibrey nanism and role for RING finger protein TRIM37 in the pathogenesis of ovarian fibrothecomas
• Hormonal alopecia in dogs and cats
• How often do we incidentally find a fetal abnormality at the routine third-trimester growth scan? A population-based study
• IGF2/H19 hypomethylation in a patient with very low birthweight, preocious pubarche and insulin resistance
• Ignored adult primary hypothyroidism presenting chiefly with persistent ovarian cysts: a need for increased awareness
• Impaired ovarian ecdysone synthesis of Drosophila melanogaster insulin receptor mutants
• Induction of ovulation and pregnancy in a pituitary dwarf
• Insulin-like growth factor-I (IGF-I) may not be essential for ovarian follicular development: evidence from IGF-I deficiency
• Investigation of a unique male and female sibship with Kallmann's syndrome and 46,XX gonadal dysgenesis with short stature
• Irofulven cytotoxicity depends on transcription-coupled nucleotide excision repair and is correlated with XPG expression in solid tumor cells
• Isosexual precocity
• Kabuki make-up syndrome in a Caucasian
• Late diagnosis of severe long-standing autoimmune hypothyroidism after the first lockdown for the Covid-19 pandemic: clinical features and follow-up
• Leprechaunism: in vitro insulin action despite genetic insulin resistance
• Loss of heterozygosity of nucleotide excision repair factors in sporadic ovarian, colon and lung carcinomas: implication for their roles of carcinogenesis in human solid tumors
• Loss-of-Function of a Tomato Receptor-Like Kinase Impairs Male Fertility and Induces Parthenocarpic Fruit Set
• Managing anesthesia for a woman with Donohue syndrome
• MCM9 mutations are associated with ovarian failure, short stature, and chromosomal instability
• Mendelian diseases and conditions in Croatian island populations: historic records and new insights
• Nanism caused by ovarian agenesia: Turner syndrome
• New method for the determination of 7 fractions of 17-deoxycorticosteroid (DOC, Comp. B, Comp. A, allo THB, THB, THA and aldosterone) and their urinary excretion. 2. Urinary excretion during normal menstrual cycle and in patients with various disease
• Ovarian agenesis with dwarfism
• Ovarian dwarfism with pituitary tumor
• Ovarian dwarfism, Turner's syndrome
• Ovarian imbalance in a German Shepherd dwarf
• Ovarian transcriptome associated with reproductive senescence in the long-living Ames dwarf mice
• Partial short arm deletions of the X chromosome and spontaneous pubertal development in girls with short stature
• Pathologic conditions in pregnancy. Preliminary evaluation of the effectiveness of magnetic resonance
• Pathophysiology of reproductive failure after clomiphene-induced ovulation
• Pituitary function test using synthetic lysine-8-vasopressin--comparison with metopirone test and insulin stress test
• Precocious puberty by tumor granulosa cells of the ovary
• Preimplantation genetic diagnosis for achondroplasia: genetics and gynaecological limits and difficulties
• Premature ovarian insufficiency and early depletion of the ovarian reserve in the monogenic Mulibrey nanism disorder
• Pseudoisodicentric Xp chromosome [46,X,psu idic(X)(q21.1)] and its effect on growth and pubertal development
• Pure Choriocarcinoma of the Ovary in Silver-Russell Syndrome
• Radioimmunoassay of serum testosterone--results of the study of normal subjects and patients with endocrine disorders
• Rapid DNA Synthesis During Early <em>Drosophila</em> Embryogenesis Is Sensitive to Maternal Humpty Dumpty Protein Function
• Rare clinical features of the Ellis van Creveld syndrome: A case report and literature review
• Recombinant human growth hormone acts on intermediate-sized follicles and rescues growing follicles from atresia
• Reproductive aging and MCM8/9
• Specific PIWI-Interacting RNAs and Related Small Noncoding RNAs Are Associated With Ovarian Aging in Ames Dwarf (df/df) Mice
• Spontaneous pregnancies in two women with Laron-type dwarfism: are growth hormone and circulating insulin-like growth factor mandatory for induction of ovulation?
• Sublingual thyroid tissue and ovarian tumor: is it more than a coincidence?
• Successful polar body-based preimplantation genetic diagnosis for achondroplasia
• Suprahypophyseal dysfunction in a patient with asexual ateleiosis
• Syndrome of ovarian agenesis (congenitally aplastic ovaries): short stature, multiple congenital abnormalities and high urinary gonadotropins in a two year, eight month old female
• Syndrome of ovarian agenesis and so-called renal nanism
• The Cockayne syndrome group B DNA repair protein as an anti-cancer target
• The diagnostic significance of parabasal cells. I. Correlation with the clinical diagnosis in 209 patients
• The importance of basonuclin 2 in adult mice and its relation to basonuclin 1
• The longitudinal course of two cases with cretinism diagnosed after adolescence
• The phenotype and rhGH treatment response of ring Chromosome 15 Syndrome: Case report and literature review
• The syndrome of congenitally aplastic ovaries with sexual infantilism, high urinary gonadotropins, short stature and other congenital abnormalities; tabular presentation of 25 previously unpublished cases
• The syndrome of ovarian agenesis and dwarfism
• Treatment of dwarfism in Turner's syndrome (ovarian dysgenesis)
• Two cases of dwarfism with total ovarian failure and hypersecretion of gonadotropic hormone; Turner's syndrome
• Two novel mutations in the MCM8 gene shared by two Chinese siblings with primary ovarian insufficiency and short stature
• Van Wyk-Grumbach syndrome: A case report and 
literature review