References
- Drachman DB, Banker BQ. Arthrogryposis multiplex con-genita: A case due to disease of the anterior horn cells. Arch Neurol 1961;5:89–105.
- Attia-Sobol J, Plauchu H, Encha-Razavi F, et al. Lissence-phaly type III, stippled epiphyses and loose, thick skin: a new recessively inherited syndrome. Am J Med Genet 2001;15,99(1):14–20.
- Hall JG. Analysis of Pena Shokeir phenotype. Am J Med Genet 1986;25(1):99–117.
- Swaiman KF. Anterior horn cell and cranial motor neuron disease. In: Swaiman KF, editor. Pediatric neurology. Principles and practice. St Louis: Mosby-Year-Book; 1994.
- Vestermark B. Arthrogryposis multiplex congenita. A case of neurogenic origin. Acta Paediatr Scand. 1966;55(1):117–120.
- Cox PM, Brueton LA, Murphy KW, et al. Early-onset fetal hydrops and muscle degeneration in siblings due to a novel variant of type IV glycogenosis. Am J Med Genet 1999;10,86(2):187–193.
- Mease AD, Yeatman GW, Pettett G, et al. A syndrome of ankylosis, facial anomalies and pulmonary hypoplasia second-ary to fetal neuromuscular dysfunction. Birth Defects Orig Artic Ser 1976;12(5):193–200.
- Moerman P, Fryns JP, Cornelis A, et al. Pathogeneis of lethal multiple pterygium syndrome. Am J Med Genet 1990;35(3):415–421.
- Moerman P, Lammens M, Fryns JP, et al. Fetal akinesia sequence caused by glycogenosis type VII. Genet Couns 1995;6(1):15–20.
- Sanoudou D, Beggs AH. Clinical and genetic heterogeneity in nemaline myopathy-a disease of skeletal muscle thin fila-ments. Trends Mol Med 2001;7(8):362–368.
- van Noort G, Straks W, Van Diggelen 0, et al. A congenital variant of glycogenosis type IV. Pediatr Pathol 1993; 13(5):685–698.
- Hecht F, Beals RK. "New" syndrome of congenital contrac-tural arachnodactyly originally described by Marfan in 1896. Pediatrics 1972;49(4):574–579.
- Charles A, Moulinasse R, Versailles L. Harlequin fetus and micromelia. Prenat Diagn 1989;9(10):709–713.
- Chen H, Blackburn WR, Wertelecki W. Fetal akinesia and multiple perinatal fractures. M J Med Genet 1995; 13,55(4):472–477.
- Thompson E, Donnai D, Baraitser M, et al. Multiple pterygium syndrome: evolution of the phenotype. J Med Genet 1987;24(12):733–749.
- Carnevale A, Hernandez AL, De los Cobos L. Sindrome de pterygium familiar con probable transmission dominante ligada al cromosoma X. Rev Invest Clin 1973;25:237–244.
- Langley FA. The perinatal postmortem examination. J Clin Pathol 1971;24(2):159–169.
- Murray PD, Drachman DB. The role of movement in the development of joints and related structures: the head and neck in the chick embryo. J Embryol Exp Morphol 1969;22(3):349–371.
- Moessinger AC. Fetal akinesia deformation sequence: an animal model. Pediatrics 1983;72(6):857–863.
- Goldstein JD, Reid LM. Pulmonary hypoplasia resulting from phrenic nerve agenesis and diaphragmatic amyoplasia. J Pediatr 1980;97(2):282–287.
- Moessinger AC, Blanc WA, Marone PA, Polsen DC. Umbilical cord length as an index of fetal activity: experi-mental study and clinical implications. Pediatr Res 1982;16(2):109–112.