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| Q34138908 | A novel chromosomal translocation t(1;14)(q25;q32) in pre-B acute lymphoblastic leukemia involves the LIM homeodomain protein gene, Lhx4. |
| Q48234928 | A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency |
| Q40631830 | Aberrant expression of the LHX4 LIM-homeobox gene caused by t(1;14)(q25;q32) in chronic myelogenous leukemia in biphenotypic blast crisis |
| Q57632741 | Bases Genéticas dos Distúrbios de Crescimento |
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| Q37078042 | Clinical manifestations of impaired GnRH neuron development and function |
| Q31055358 | Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion. |
| Q36021378 | Comparative genomics reveals functional transcriptional control sequences in the Prop1 gene |
| Q34997016 | Current approaches for deciphering the molecular basis of combined anterior pituitary hormone deficiency in humans |
| Q35197885 | DNA testing in patients with GH deficiency at the time of transition |
| Q41870341 | Delayed puberty due to pituitary stalk dysgenesis and ectopic neurohypophysis. |
| Q90260818 | Development of the Pituitary Gland |
| Q53280917 | Downregulation of alpha-fetoprotein expression by LHX4: a critical role in hepatocarcinogenesis. |
| Q84342777 | Ectopic posterior pituitary and stalk abnormality predicts severity and coexisting hormone deficiencies in patients with congenital growth hormone deficiency |
| Q34000427 | Epigenomic and transcriptomic signatures of a Klinefelter syndrome (47,XXY) karyotype in the brain |
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| Q35668777 | From panhypopituitarism to combined pituitary deficiencies: do we need the anterior pituitary? |
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| Q89687374 | Genetic causes of hypopituitarism |
| Q33698242 | Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari type I malformation |
| Q33590141 | Genetic regulation of pituitary gland development in human and mouse |
| Q38797075 | Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era. |
| Q90569848 | Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease |
| Q28300499 | Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency |
| Q34430600 | Gradual loss of ACTH due to a novel mutation in LHX4: comprehensive mutation screening in Japanese patients with congenital hypopituitarism |
| Q36214845 | Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter? |
| Q34158374 | HESX1 and Septo-Optic Dysplasia |
| Q48320173 | Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe |
| Q35964450 | Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency |
| Q31141847 | Hypopituitarism oddities: congenital causes |
| Q91584316 | Hypothalamic-pituitary magnetic resonance imaging in growth hormone deficiency |
| Q36107279 | ISL1 Is Necessary for Maximal Thyrotrope Response to Hypothyroidism |
| Q35754297 | Inherited adrenal hypoplasia: not just for kids! |
| Q51945810 | Interstitial 1q25.3‐q31.3 deletion in a boy with mild manifestations |
| Q36196340 | LIM-homeodomain genes in mammalian development and human disease. |
| Q30947967 | Magnetic resonance imaging of the hypothalamus-pituitary unit in childrensuspected of hypopituitarism: who, how and when toinvestigate |
| Q33630319 | Mechanisms for pituitary tumorigenesis: the plastic pituitary |
| Q51968780 | Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency. |
| Q34622336 | Molecular analysis of the PROP1 and HESX1 genes in patients with septo-optic dysplasia and/or pituitary hormone deficiency |
| Q38132737 | Molecular and Clinical Findings in Patients with LHX4 and OTX2 Mutations |
| Q31017898 | Molecular and evolutionary analysis of the growth-controlling region on the human Y chromosome |
| Q36066626 | Molecular defects in the growth hormone-IGF axis |
| Q34017922 | Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes. |
| Q48849523 | Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD). |
| Q82030022 | Neuroendocrine complications of central nervous system malformations |
| Q49653037 | Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities |
| Q34367104 | Novel insights into the aetiology and pathogenesis of hypopituitarism |
| Q34992939 | Other transcription factors and hypopituitarism |
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| Q31035731 | Phenotypic variability in children with growth hormone deficiency associated with posterior pituitary ectopia |
| Q90540512 | Pituitary Transcription Factor Mutations Leading to Hypopituitarism |
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| Q54483003 | Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1. |
| Q36885537 | Pituitary development and physiology |
| Q33687947 | Pituitary gland development and disease: from stem cell to hormone production |
| Q34544745 | Pituitary stalk interruption syndrome in 53 postpubertal patients: factors influencing the heterogeneity of its presentation |
| Q43750873 | Pituitary stalk interruption syndrome in 58 Chinese patients: clinical features and genetic analysis |
| Q43536332 | Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly |
| Q35058034 | Renal anomalies associated with ectopic neurohypophysis |
| Q35754081 | Roles of the LHX3 and LHX4 LIM-homeodomain factors in pituitary development. |
| Q28395683 | Salicylate-induced degeneration of cochlea spiral ganglion neurons-apoptosis signaling |
| Q48914772 | Septo-optic-pituitary dysplasia |
| Q37633655 | Stem cells in the pituitary gland: A burgeoning field |
| Q36751719 | Stem cells in the postnatal pituitary? |
| Q36659067 | The (epi)genetics of human synovial sarcoma |
| Q80715463 | The C terminus of the synovial sarcoma-associated SSX proteins interacts with the LIM homeobox protein LHX4 |
| Q47107088 | The Missing Link: A Case of Absent Pituitary Infundibulum and Ectopic Neurohypophysis in a Pediatric Patient with Heterotaxy Syndrome |
| Q35946579 | The adrenal |
| Q47707976 | The de novo Q167K mutation in the POU1F1 gene leads to combined pituitary hormone deficiency in an Italian patient |
| Q37456706 | The molecular basis of hypopituitarism |
| Q37905532 | The role of homeodomain transcription factors in heritable pituitary disease |
| Q36793669 | The role of transcription factors implicated in anterior pituitary development in the aetiology of congenital hypopituitarism |
| Q34033813 | The use of neuroimaging for assessing disorders of pituitary development. |
| Q36494440 | Three novel missense mutations within the LHX4 gene are associated with variable pituitary hormone deficiencies. |
| Q35575317 | Transcriptional control during mammalian anterior pituitary development |
| Q46501386 | Unilateral agenesis of internal carotid artery associated with congenital combined pituitary hormone deficiency and pituitary stalk interruption without HESX1, LHX4 or OTX2 mutation: a case report. |
| Q36473963 | Unusual phenotypic features in a patient with a novel splice mutation in the GHRHR gene |
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