"blue sclerae"

Key Phrases: Invest Dermatol, Cell Biol, Biol Chem, Arch Dermatol, New York, Cancer Res, tumor cell chemotaxis, restrictive dermatopathy, congenital fascial dystrophy, enlarged fascia, chronic bullous disease, oral blisters (see more)

Key Phrases: Invest Dermatol, Cell Biol, Biol Chem, Arch Dermatol, New York, Cancer Res, Academic Press, Proc Natl Acad Sci, Clin Invest, Lab Invest, Med Genet, Cell Physiol, Arthritis Rheum, Exp Cell Res, Harcourt Brace Jovanovich, Ann Intern Med, Exp Med, Biochim Biophys Acta, Hum Genet, Biochem Biophys Res Commun, Bioeng Skin, Cell Biochem, Clin Exp Dermatol, Clinical Research Centre, Michael Pope, tumor cell chemotaxis, restrictive dermatopathy, congenital fascial dystrophy, enlarged fascia, chronic bullous disease, oral blisters, cutis laxa, systemic glucocorticoid treatment, fibroblast chemotaxis, dermal equivalent, cutaneous striae, tumor cell invasion, scleroderma fibroblasts, eosinophilic fasciitis, injectable collagen, fibroblastic cells, scleroderma skin, anchoring fibrils, systemic scleroderma, cutaneous changes, fibroblast activity, blue sclerae, collagenase expression, angioid streaks, pathologic situations (see less)

Key Phrases: Birth Date, Number Refer, Brachmann-de Lange, Circulatory Cardiac, United States, Learning Cognitive, preventive medical checklist, repeat every decade, poli ovirus, percent recurrence risk, spina bifida team, craniofacial surgery team (see more)

Key Phrases: Birth Date, Number Refer, Brachmann-de Lange, Circulatory Cardiac, United States, Learning Cognitive, Treacher Collins, Excretory Renal, American Academy of Pediatrics, Number Pediatric Screen Evaluate Refer, New York, American Journal of Medical Genetics, Cranial Microcephaly, Growth Short, Axial Scoliosis, Cranial Macrocephaly, Behavior Behavior, Growth Low, Motor Hypotonia, Mouth Oromotor, Pierre Robin, San Filippo, Sensory Vision, Consensus Development Conference, Cornelia de Lange, preventive medical checklist, repeat every decade, poli ovirus, percent recurrence risk, spina bifida team, craniofacial surgery team, varic ella, skeletal radiographic survey, minimal recurrence risk, patients with cleft palate, ntal monitoring, periodic urinalyses, audiology screening, preventive management, arthrogryposis syndromes, syn rome, alternative timing, exhibit autosomal recessive inheritance, oculocutaneous albinism type, havioral issues, labial hypoplasia, neonatal evaluation, craniofacial team, syndrome checklist, genetic referral (see less)

Key Phrases: Bone Miner Res, Clin Invest, Clin Endocrinol Metab, Biol Chem, Calcif Tissue Int, New York, sclerosing bone dystrophy, pagetic subjects, adjusted apposition rate, hyperparathyroid bone disease, calcitonin receptor isoforms, atypical osteomalacia (see more)

Key Phrases: Bone Miner Res, Clin Invest, Clin Endocrinol Metab, Biol Chem, Calcif Tissue Int, New York, Ann Intern Med, Kidney Int, Proc Natl Acad Sci, Med Genet, Color Plate, Arch Intern Med, Hum Genet, Atlas of Mineralized Bone Histology, Clin Orthop, United States, Clin Nutr, Dis Child, Arthritis Rheum, Osteoporosis Int, Nat Genet, Ann Rheum Dis, Biochem Biophys Res Commun, Miner Electrolyte Metab, Raven Press, sclerosing bone dystrophy, pagetic subjects, adjusted apposition rate, hyperparathyroid bone disease, calcitonin receptor isoforms, atypical osteomalacia, parathyroid gland weight, phosphate binders containing aluminum, pagetic bone, patients with hypoparathyroidism, renal hypercalciuria, gyro mice, renal filtered load, uremic bone disease, osteoid seam thickness, bovine parathyroid cells, osteoid accumulation, axial osteomalacia, disodium etidronate therapy, hereditary hypophosphatemia, hypophosphatemic patients, intermittent versus continuous administration, pagetic patients, woven osteoid, hyp mice (see less)

Key Phrases: Inheritance Autosomal, Inherited Syndromic Hearing Impairment, Genes Unknown Mutational, Chromosomal Mitochondrial, Epidemiology Unknown, Inheritance Maternal, mixed hearing impairment, conductive hearing impairment, enlarged vestibular aqueduct, molecular gene tics, nonsyndromic hearing impairment, broad big toes (see more)

Key Phrases: Inheritance Autosomal, Inherited Syndromic Hearing Impairment, Genes Unknown Mutational, Chromosomal Mitochondrial, Epidemiology Unknown, Inheritance Maternal, Inherited Diseases, Inheritance X-linked, Diagnosis Mutation, Chromosomal Unknown, Clinicalfeatures Progressive, Diagnosis Clinical, Diagnosis Diagnosis, Diagnosis Family, Inheritance Most, Mohr Tranebjaerg, Pierre Robin, mixed hearing impairment, conductive hearing impairment, enlarged vestibular aqueduct, molecular gene tics, nonsyndromic hearing impairment, broad big toes, neck paragangliomas, counseling issues, carotid body tumors, contiguous gene syndrome, maternal pattern, mutation analysis, protein truncation, profound hearing impairment, internal auditory canal, vestibular responses, velocardiofacial syndrome, cochlear implantation, conductive component, blue sclerae, maxillary hypoplasia, pigmentary retinopathy, vestibular dysfunction, mitochondrial mutations, choanal atresia (see less)