Atkinson, 1937, Hereditary craniofacial dysostosis or Crouzon's disease, Med Press Circular, 195, 118
Barr, 1995, Craniomicromelic syndrome: a newly recognized lethal condition with craniosynostosis, distinct facial anomalies, short limbs, and intrauterine growth retardation, Am J Med Genet, 58, 348, 10.1002/ajmg.1320580409
Bugge, 1994, Monozygotic twins discordant for gastroschisis: case report and review of the literature of twins and familial occurrence of gastroschisis, Am J Med Genet, 52, 223, 10.1002/ajmg.1320520219
Calzolari, 1995, Omphalocele and gastroschisis in Europe: a survery of 3 million births 1980-1990, Am J Med Genet, 58, 187, 10.1002/ajmg.1320580218
Camera, 1993, Holoprosencephaly and primary craniosynostosis: the Genoa syndrome, Am J Med Genet, 47, 1161, 10.1002/ajmg.1320470806
Charnas, 1989, Crouzon syndrome: evidence of incomplete penetrance, Am J Med Genet, 45S, 43
Chumas, 1997, Classification of previously unclassified cases of craniosynostosis, J Neurosurg, 86, 177, 10.3171/jns.1997.86.2.0177
Cinalli, 1995, Chronic tonsillar herniation in Crouzon's and Apert's syndromes: the role of premature synostosis of the Lmbdoid suture, J Neurosurg, 83, 575, 10.3171/jns.1995.83.4.0575
Cohen, 1986, Syndromes with craniosynostosis, 413
Cohen, 1992, Birth prevalence studies of the Crouzon syndrome: comparison of direct and indirect methods, Clin Genet, 41, 12, 10.1111/j.1399-0004.1992.tb03620.x
Cohen, 1996, Lambdoid synostosis is an overdiagnosed condition, Am J Med Genet, 61, 98, 10.1002/ajmg.1320610109
Cormier Daire, 1995, Craniosynostosis and kidney malformation in a case of Hennekam syndrome, Am J Med Gent, 22, 66, 10.1002/ajmg.1320570115
Cross, 1969, Craniosynostosis in the Amish, J Pediatr, 75, 1037, 10.1016/S0022-3476(69)80343-4
Cunniff, 1990, Cranuosynostosis and lid anomalies: report of a girl with Michels syndrome, Am J Med Genet, 37, 28, 10.1002/ajmg.1320370108
Drongowski, 1991, Contribution of demographic and environmental factors to the etiology of gastroschisis: a hypothesis, Fetal Diagn Ther, 6, 14, 10.1159/000263620
Eppley, 1995, Resorbable coupling fixation in craniosynostosis surgery: experimental and clinical applications, J Craniofac Surg, 6, 477, 10.1097/00001665-199511000-00011
Frydman, 1984, Trigonocephlay: A New Familial Syndrome, Am J Med Gen, 18, 55, 10.1002/ajmg.1320180109
Greitzer, 1974, Craniosynostosis-radial aplasia syndrome, J Pediatr, 84, 4, 10.1016/S0022-3476(74)80017-X
Haddow, 1993, Young maternal age and smoking during pregnancy as risk factors for gastroschisis, Teratology, 47, 225, 10.1002/tera.1420470306
Hassell, 1994, Antley-Bixler syndrome: report of a patient and review of literature, Clin Genet, 46, 372, 10.1111/j.1399-0004.1994.tb04182.x
Ilyina, 1990, Dubowitz syndrome: possible evidence for a clinical subtype, Am J Med Genet, 35, 561, 10.1002/ajmg.1320350423
Jabs, 1993, A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis, Cell, 75, 443, 10.1016/0092-8674(93)90379-5
Jabs, 1994, Jackson-Weiss and Crouzon syndromes are allelic with muta tions in fibroblast growth factor receptor 2, Nat Genet, 8, 9, 10.1038/ng1194-275
Jones, 1997, Craniosynostosis syndromes, 31
Juberg, 1973, An autosomal recessive form of craniofacial dysostosis (the Crouzon syndrome), J Med Genet, 10, 89, 10.1136/jmg.10.1.89
Kaplan, 1988, A new acro-cranio-facial dysostosis syndrome in sisters, Am J Med Genet, 29, 95, 10.1002/ajmg.1320290112
Khiem, 1969, Malformations r6nales et maladie de Crouzon, Acta Urologica Belgica, 37, 149
Koppe, 1989, Ambiguous genitalia associated with skeletal abnormalities, cutis laxa, craniostenosis, psychomotit retardation, and facial abnormalities (SCARF syndrome), Am J Med Genet, 34, 305, 10.1002/ajmg.1320340302
Kreiborg, 1981, Crouzon syndrome, Scand J Plast Reconstr Surg, 18, 1
Lambert, 1983, Cutis laxa generalis6e congenitale, Ann Dermatol Venereol, 110, 129
Levin, 1977, A heritable syndrome of craniosynostosis, short thin hair, abnormalities, and short limbs: cranioectodermal dysplasia, J Pediatr, 90, 55, 10.1016/S0022-3476(77)80764-6
Lin, 1993, Further delineation of the Baller-Gerold syndrome, Am J Med Genet, 45, 519, 10.1002/ajmg.1320450423
Lowry, 1972, Congenital absence of the fibula and craniosynostosis in sibs, J Med Genet, 9, 227, 10.1136/jmg.9.2.227
Ludman, 1993, Hypomandibular faciocranial dysostosis: another case and review, Am J Med Genet, 47, 352, 10.1002/ajmg.1320470311
Mc Kusick, 1996, Online Mendelian inheritance in man, OMIM (TM)
Menashe, 1989, Exophthalsmus-Prenatal ultrasonic features for diagnosis of Crouzon Syndrome, Prenat Diagn, 9, 805, 10.1002/pd.1970091109
Meyers, 1995, Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans, Nat Genet, 11, 462, 10.1038/ng1295-462
Muhlbauer, 1989, Early operation in craniofacial dysostosis, World J Surg, 13, 366, 10.1007/BF01660749
Nevin, 1994, An 18 week fetus with Elejalde syndrome (acrocephalopolydactylyous dysplasia), Clin Dysmorphol, 3, 180, 10.1097/00019605-199404000-00017
Neuhauser, 1976, Studies of malformation syndromes of man XXXIX: a craniosynostosis-craniofacial dysostosis with mental retardation and other malformations: "craniofacial dyssynostosis", Eur J Pediatr, 123, 15, 10.1007/BF00497676
Parent, 1996, Le nanisme a t6te d'oiseau ou syndrome de Seckel, Difficult6s nosologiques. Arch Pediatr, 3, 55, 10.1016/S0929-693X(96)80011-X
Pelias, 1981, Brief clinical report: a sixth report (eighth case) of craniosynostosis-radial aplasia (Baller-Gerold) syndrome, Am J Med Genet, 10, 133, 10.1002/ajmg.1320100206
Preis, 1995, Gorlin-ChaudhryMoss or Saethre-Chotzen syndrome?, Clin Genet, 47, 9
Reardon, 1994, Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome, Nat Genet, 8, 98, 10.1038/ng0994-98
Reichenbach, 1993, Ein weiterer Fall mit Baller-Gerold-Syndrom (Craniosynostosis - Radial Aplasia Syndrome) - Uberblick and neue Ge sichtspunkte bei einem seltenen Syndrom, Kinderarztl Prax, 61, 161
Richieri-Costa, 1993, Newly recognized autosomal recessive MCA/MR/ overgrowth syndrome, Am J Med Genet, 47, 278, 10.1002/ajmg.1320470227
Rollnick, 1988, Germinal mosaicism in Crouzon syndrome, Clin Genet, 33, 145, 10.1111/j.1399-0004.1988.tb03429.x
Schinzel, 1983, Antley-Bixler Syndrome in Sisters: A Term Newborn and a Prenatally Diagnosed Fetus, Am J Med Genet, 14, 139, 10.1002/ajmg.1320140119
Shiller, 1959, Craniofacial dysostosis of Crouzon: a case report and pedigree with emphasis on heredity, Pediatrics, 23, 107, 10.1542/peds.23.1.107
Singer, 1991, Fetal Growth and Maturation: with Standards for Body and Organ Development, Vol. 1, 11
Stratton, 1990, C syndrome with apparently normal development, Am J Med Genet, 37, 460, 10.1002/ajmg.1320370406
Wagstaff, 1995, A Familial "Balanced" 3; 9 Translocation with Cryptic 8q Insertion Leading to Deletion and Duplication of 9p23 Loci in Siblings, Am J Hum Genet, 56, 302
Werler, 1992, First trimester maternal medication use in relation to gastroschisis, Teratology, 45, 361, 10.1002/tera.1420450407
Werler, 1992, Demographic, reproductive, medical, and environmental factors in relation to gastroschisis, Teratology, 45, 353, 10.1002/tera.1420450406
Young, 1992, Genetic -epidemiologic study of omphalocele and gastroshisis: evidence for heterogeneity, Am J Med Genet, 45, 668, 10.1002/ajmg.1320440528