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Factors that affect coping with turner syndrome
JOURNAL OF NURSING SCHOLARSHIP
Molecular analysis of genes on Xp controlling turner syndrome and premature ovarian failure (POF)
SEMINARS IN REPRODUCTIVE MEDICINE
Ring X and other structural X chromosome abnormalities: X inactivation andphenotype
SEMINARS IN REPRODUCTIVE MEDICINE
The human Y chromosome, in the light of evolution
NATURE REVIEWS GENETICS
X chromosome inactivation patterns in 45,X/46,XX mosaics
JOURNAL OF HUMAN GENETICS
Where and what visuospatial processing in adolescents with congenital hypothyroidism
JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY
Turner's syndrome and fertility: current status and possible putative prospects
HUMAN REPRODUCTION UPDATE
Long-term results of growth hormone therapy in Turner syndrome
ENDOCRINE
A short pseudoautosomal region in laboratory mice
GENOME RESEARCH
The X chromosome and the ovary
JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION
Vertebral artery dissection in Turner's syndrome: Diagnosis by magnetic resonance imaging
JOURNAL OF NEUROIMAGING
Estrogen and related compounds: Biphasic dose responses
CRITICAL REVIEWS IN TOXICOLOGY
Turner's syndrome, melanocytic nevi and melanoma
DERMATOLOGY
Nevi and melanoma: Lessons from Turner's syndrome
DERMATOLOGY
Different chromosome Y abnormalities in Turner syndrome
GENETIC COUNSELING
Growth hormone and gonadotropin-releasing hormone analog therapy in haploinsufficiency of SHOX
ENDOCRINE JOURNAL
Sleep apnoea and Turner's syndrome
EUROPEAN RESPIRATORY JOURNAL
Behavioral phenotypes of genetic syndromes: A reference guide for psychiatrists
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes
GENOMICS
A complete map of the human ribosomal protein genes: Assignment of 80 genes to the cytogenetic map and implications for human disorders
GENOMICS
Parsonage-Turner syndrome after total-hip arthroplasty
JOURNAL OF ARTHROPLASTY
Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trial
ACTA PAEDIATRICA
Morning versus evening administration of estradiol to girls with Turner syndrome receiving growth hormone: impact on growth hormone and metabolism. Arandomized placebo-controlled crossover study
ACTA PAEDIATRICA
Perinatal 'programming' of insulin resistance in childhood: critical impact of neonatal insulin and low birth weight in a risk population
DIABETIC MEDICINE
SHOX gene in Leri-Weill syndrome and in idiopathic short stature
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
The human Y chromosome: function, evolution and disease
FORENSIC SCIENCE INTERNATIONAL
Estrogen receptors in the normal adult and developing human inner ear and in Turner's syndrome
HEARING RESEARCH
Analysis of short stature homeobox-containing gene (SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity
HUMAN GENETICS
Short stature as the only presenting feature in a patient with an isodicentric (Y)(q11.23) and gonadoblastoma. A clinical and molecular cytogenetic study
EUROPEAN JOURNAL OF PEDIATRICS
Height velocity in Argentinean girls with Turner's syndrome
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
IGF-I resistance and Turner's syndrome
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
Turner's syndrome
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
Current concepts in tall stature and overgrowth syndromes
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
Radiological signs of Leri-Weill dyschondrosteosis in Turner syndrome
HORMONE RESEARCH
Final height in children with idiopathic growth hormone deficiency treatedwith recombinant human growth hormone: The Belgian experience
HORMONE RESEARCH
Discordant growth pattern and ovarian function in monozygotic twins with 45,X/46,XX mosaicism
HORMONE RESEARCH
SHOX in short stature syndromes
HORMONE RESEARCH
Increased prevalence of scoliosis in Turner syndrome
JOURNAL OF PEDIATRIC ORTHOPAEDICS
Mapping of 12 bovine ribosomal protein genes using a bovine radiation hybrid panel
ANIMAL GENETICS
Reduced free IGF-I and increased IGFBP-3 proteolysis in Turner syndrome: modulation by female sex steroids
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
Women with Turner syndrome: psychological well-being, self-rated health and social life
JOURNAL OF PSYCHOSOMATIC OBSTETRICS AND GYNECOLOGY
Isochromosome consisting of terminal short arm and proximal long arm X in a girl with short stature
AMERICAN JOURNAL OF MEDICAL GENETICS
Atypical phenotype in a female with a large Xp deletion
AMERICAN JOURNAL OF MEDICAL GENETICS
Klinefelter syndrome and cutis verticis gyrata
AMERICAN JOURNAL OF MEDICAL GENETICS
A man who inherited his SRY gene and Leri-Weill dyschondrosteosis from hismother and neurofibromatosis type 1 from his father
AMERICAN JOURNAL OF MEDICAL GENETICS
Preliminary evidence for a cognitive phenotype in Barth syndrome
AMERICAN JOURNAL OF MEDICAL GENETICS
Kabuki syndrome-like features associated with a small ring chromosome X and XIST gene expression
AMERICAN JOURNAL OF MEDICAL GENETICS
Sex chromosome mosaicism in gonads of a fetus with cystic hygroma and deletion of the short arm of Y chromosome including loss of SRY
AMERICAN JOURNAL OF MEDICAL GENETICS
Short stature in a mother and daughter caused by familial der(X)t(X;X)(p22.1-3;q26)
AMERICAN JOURNAL OF MEDICAL GENETICS
Cytogenetic and molecular characterization of two isodicentric Y chromosomes
AMERICAN JOURNAL OF MEDICAL GENETICS
Congenital heart defects in Kabuki syndrome
AMERICAN JOURNAL OF MEDICAL GENETICS
Is the handedness gene on the X chromosome? Comment on Jones and Martin (2000)
PSYCHOLOGICAL REVIEW
Effect of estrogen therapy on the growth of Turner Syndrome girls treated with growth hormone.
MEDICINA-BUENOS AIRES
Intraoperative endoscopy in a child with Turner's syndrome and gastrointestinal hemorrhage: A case report
JOURNAL OF PEDIATRIC SURGERY
Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location
JOURNAL OF MEDICAL GENETICS
Coeliac disease in Williams syndrome
JOURNAL OF MEDICAL GENETICS
SHOX haploinsufficiency and overdosage: impact of gonadal function status
JOURNAL OF MEDICAL GENETICS
Point mutation in essential genes with loss or mutation of the second allele: Relevance to the retention of tumor-specific antigens
JOURNAL OF EXPERIMENTAL MEDICINE
Comment on "Editorial: The role of androgens in women"
JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
Annotation: The cognitive neuroscience of face recognition: Implications for developmental disorders
JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES
Intrauterine growth restriction. Some chromosomal, genetic and exogenic causes
GYNAKOLOGE
PCR-PRINS-FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype
CLINICAL GENETICS
A non-sex chromosome marker in a patient with an atypical Ullrich-Turner phenotype and mosaicism of 46,X,mar/46,XX
CLINICAL GENETICS
Deletion of the factor IX gene as a result of translocation t(X;1) in a girl affected by haemophilia B
BRITISH JOURNAL OF HAEMATOLOGY
Short stature in Noonan syndrome: response to growth hormone therapy
ARCHIVES OF DISEASE IN CHILDHOOD
A multicentre trial of recombinant growth hormone and low dose oestrogen in Turner syndrome: near final height analysis
ARCHIVES OF DISEASE IN CHILDHOOD
A case of (X;15) translocation diagnosed as a paracentric inversion of Xp:diagnostic revision with FISH
ANNALES DE GENETIQUE
An infant with Turner-Down aneuploidy and massive capillary hemangioma of the orbit: a case report with review
ANNALES DE GENETIQUE
Cell-cycle kinetics of cell lines from patients with chromosomal mosaicism
ANNALES DE GENETIQUE
The effect of growth hormone on craniofacial growth and dental maturation in Turner syndrome
ANGLE ORTHODONTIST
X chromosome genes and premature ovarian failure
SEMINARS IN REPRODUCTIVE MEDICINE
Premature ovarian failure and the FMR1 gene
SEMINARS IN REPRODUCTIVE MEDICINE
The human ribosomal protein L6 gene in a critical region for Noonan syndrome
JOURNAL OF HUMAN GENETICS
Investigation of a cluster of children with Down's syndrome born to mothers who had attended a school in Dundalk, Ireland
OCCUPATIONAL AND ENVIRONMENTAL MEDICINE
Bone mineral metabolism in patients with Turner's syndrome treated with GH and estrogen: cross-sectional and longitudinal data
Italian journal of mineral and electrolyte metabolism
Safety issues in children and adolescents during growth hormone therapy - a review
GROWTH HORMONE & IGF RESEARCH
The mouse brain transcriptome by SAGE: Differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals
GENOME RESEARCH
Brain imaging in neurogenetic conditions: Realizing the potential of behavioral neurogenetics research
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
Advances in research on the fragile X syndrome
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
Neurobehavioral phenotype of Klinefelter syndrome
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
Neurodevelopmental and psychosocial aspects of Turner syndrome
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
Ribosomal protein S19 gene mutations in patients with Diamond-Blackfan anemia and identification of ribosomal protein S19 pseudogenes
BLOOD CELLS MOLECULES AND DISEASES
Children with chronic conditions: The importance of growth assessment
NURSE PRACTITIONER FORUM-CURRENT TOPICS AND COMMUNICATIONS
Genetic studies in idiopathic short stature
CURRENT OPINION IN PEDIATRICS
Selective T-cell deficiency in Turner's syndrome
JOURNAL OF INVESTIGATIONAL ALLERGOLOGY & CLINICAL IMMUNOLOGY
Examination of trisomy 13, 18 and 21 foetal tissues at different gestational ages using FISH
EUROPEAN JOURNAL OF HUMAN GENETICS
Phenotypic variation and genetic heterogeneity in Leri-Weill syndrome
EUROPEAN JOURNAL OF HUMAN GENETICS
Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements
EUROPEAN JOURNAL OF HUMAN GENETICS
Discrepancy between cytogenetic and FISH results on an amniotic fluid sample of 45,X/46,X,idic(Y)(p11)
FETAL DIAGNOSIS AND THERAPY
Usefulness of fluorescence in situ hybridization for the diagnosis of turner mosaic fetuses with small ring X chromosomes
FETAL DIAGNOSIS AND THERAPY
Spontaneous cerebral haemorrhage without hypertension in non-mosaic 45X Turner's syndrome
JOURNAL OF CLINICAL NEUROSCIENCE
Prognostic value of ultrasound findings of fetal cystic hygroma detected in early pregnancy by transvaginal sonography
ULTRASOUND IN OBSTETRICS & GYNECOLOGY
Cirrhosis in Turner's syndrome: case report and literature review
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
A case of 45,X Turner syndrome with spontaneous ovulation proven by ultrasonography
GYNECOLOGICAL ENDOCRINOLOGY
Chromosomal domains and escape from X inactivation: comparative X inactivation analysis in mouse and human
MAMMALIAN GENOME
Multicystic kidney dysplasia and Turner syndrome: two cases and a literature review
PEDIATRIC NEPHROLOGY
Frequency of renal malformations in Turner syndrome: analysis of 82 Turkish children
PEDIATRIC NEPHROLOGY
Autoimmune thyroiditis in children with Turner syndrome
JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
Renal malformations in children with Turner's syndrome
JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
Laparoscopic removal of gonads in a Turner's syndrome mosaic female patient with isodicentric Y chromosome
INTERNATIONAL JOURNAL OF UROLOGY