| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF00441581 |
| P698 | PubMed publication ID | 7363911 |
| P2093 | author name string | B D Hall | |
| J Spranger | |||
| P2860 | cites work | Congenital bowing and angulation of long bones. | Q33968808 |
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| The Weissenbacter-Zweymuller syndrome. A case report with review of the world literatue | Q41267612 | ||
| Heterogeneity in the campomelic syndromes. Long-and short-bone varieties | Q41714151 | ||
| A rare lethal bone dysplasia with recessive autosomic transmission | Q44020672 | ||
| Congenital angulation of the lower leg and congenital pseudarthrosis of the tibia in Denmark | Q44132423 | ||
| Syndromes of congenital bowing of the long bones | Q44459064 | ||
| Femoral hypoplasia — unusual facies syndrome | Q44777837 | ||
| Limb defects in the amniotic band syndrome | Q46075768 | ||
| Prenatal bowing of long bones in two sibs | Q52319257 | ||
| [Disease picture of congenital bowing of long bones] | Q52320080 | ||
| Increasing frequency of a syndrome of multiple osseous defects? | Q52331767 | ||
| Prenatal bowing and angulation of long bones; a description of its occurrence in a brother and sister. | Q52362584 | ||
| Prenatal bowing and thickening of tubular bones, with multiple cutaneous dimples in arms and legs; a congenital syndrome of mechanical origin. | Q52370403 | ||
| Camptomelic dwarfism. A genetically determined mesenchymal disorder combined with sex reversal | Q67013316 | ||
| Dyssegmental dwarfism. A lethal anisospondylic camptomicromelic dwarfism | Q67323506 | ||
| A variant of campomelia | Q67348959 | ||
| Familial congenital bowing of the tibia with pseudarthrosis and pectus excavatum: report of a kindred | Q67783472 | ||
| Chondrodysplastic dwarfism, cleft palate and micrognathia in a neonate, a new syndrome? | Q67786083 | ||
| A severe infantile micromelic chondrodysplasia which resembles Kniest disease | Q67858991 | ||
| The campomelic syndrome. Congenital bowing of limbs and other skeletal and extraskeletal anomalies | Q69765267 | ||
| The "campomelic" syndrome. Short life-span dwarfism with respiratory distress, hypotonia, peculiar facies, and multiple skeletal and cartilaginous deformities | Q70500665 | ||
| Congenital bowing of long bones--occurrence in two sisters | Q70706796 | ||
| [The campomelic syndrome] | Q71786081 | ||
| [Ulno-fibular dysplasia. An autosome-dominant hereditary micromesomelia resembling the Nievergelt syndrome] | Q71993896 | ||
| [Prenatal bowing of the long tubular bones] | Q72236628 | ||
| Mesomelic Dwarfism of the Hypoplastic Ulna, Fibula, Mandible Type | Q72312350 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | congenital disorder | Q727096 |
| P304 | page(s) | 131-138 | |
| P577 | publication date | 1980-03-01 | |
| P1433 | published in | European Journal of Pediatrics | Q15755736 |
| P1476 | title | Congenital bowing of the long bones. A review and phenotype analysis of 13 undiagnosed cases | |
| P478 | volume | 133 |
| Q35942776 | Approach to skeletal dysplasia |
| Q40234428 | Are bowing of long tubular bones and preaxial polydactyly signs of the Meckel syndrome? |
| Q67831532 | Campomelia, polycystic dysplasia, and cervical lymphocele in two sibs |
| Q52277764 | Familial congenital bowing with short thick bones and metaphyseal changes, a distinct entity. Report of the clinical and radiological findings in two siblings. |
| Q36940668 | Fuhrmann syndrome of right-angle bowed femora, absence of fibulae and digital anomalies: Two further cases |
| Q37165242 | Osteogenesis imperfecta and clubfoot-a rare combination: Case report and review of the literature |
| Q39236186 | Oto-palato-digital syndrome type II. Report of two related cases |
| Q39804165 | Radiology and histopathology of the bent limbs in campomelic dysplasia: implications in the aetiology of the disease and review of theories |
| Q33596459 | Short stature/short limb skeletal dysplasia with severe combined immunodeficiency and bowing of the femora: report of two patients and review |
| Q51083632 | Thanatophoric dysplasia. Correlation among bone X-ray morphometry, histopathology, and gene analysis. |
| Q57384777 | Unilateral bowing of long bones and multiple congenital anomalies in a child born to a mother with gestational diabetes |
| Q70906468 | XY Sex-reversed campomelia |
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