Lammer EJ, Opitz JM: The DiGeorge anomaly as a developmental field defect. Am J Med Genet1986;2(Suppl):113-127.
2.
Palacios J., Gamallo C., Garcia M., Rodriguez JI: Decrease in thyrocalcitonin-containing cells and analysis of other congenital anomalies in 11 patients with DiGeorge anomaly. Am J Med Genet1993;46:641-646.
3.
Greenberg F. : DiGeorge syndrome: An historical review of clinical and cytogenic features. J Med Genet1993;30:803-806.
4.
Conley ME, Beckwith JB, Mancer JFK, Tenckhoff L.: The spectrum of the DiGeorge syndrome. J Pediatr1979;94:883-890.
5.
Carey JC: Spectrum of DiGeorge "syndrome." J Pediatr1980; 96:955-956.
6.
van Essen AJ, Schoots CJF, van Lingen RA, et al: Isochromosome 18q in a girl with holoprosencephaly, DiGeorge anomaly, and streak ovaries. Am J Med Genet1993;47:85-88.
7.
Shen SC, Falk RE, Swanson VL: Coexistence of Kallmann syndrome and DiGeorge syndrome, abstract. Clin Res1979;27:119A.
8.
Hong R., Horowitz SD, Borzy MF, et al: The cerebro-hepato-renal syndrome of Zellweger: Similarity to and differentiation from the DiGeorge syndrome. Thymus1981;3:97-104.
9.
Nickel RE, Pillers DM, Merkens M., et al: Velo-cardio-facial syndrome and DiGeorge sequence with meningomyelocele and deletions of the 22q11 region. Am J Med Genet1994;52:445-449.
10.
Müller W., Peter JJ, Wilden M., et al: The DiGeorge syndrome. I. Clinical evaluation and course of partial and complete forms of the syndrome. Eur J Pediatr1988;147:496-502.
11.
Shprintzen RJ: Velocardiofacial syndrome and DiGeorge sequence, letter. J Med Genet1994;31:423-424.
12.
Goldberg R. , Motzkin B., Marion R., et al: Velo-cardio-facial syndrome: A review of 120 patients. Am J med Genet1993;45:313-319.
13.
Mitnick RJ, Bello JA, Shprintzen RJ: Brain anomalies in velo-cardio-facial syndrome. Am J Med Genet1994;54:100-106.
14.
Volpe JJ: Neuronal proliferation, migration, organization, and myelination, in Neurology of the Newborn, 3rd ed. Philadelphia, WB Saunders, 1995, pp 43-94.
15.
Barkovich AJ , Chuang SH, Norman D.: MR of neuronal migration anomalies. AJR Am J Roentgenol1988; 150:179-187.
16.
Barkovich AJ , Rowley H., Bollen A.: Correlation of prenatal events with the development of polymicrogyria. AJNR Am J Neuroradiol1995;16:822-827.
17.
Richman DP, Stewart RM, Caviness VS: Cerebral microgyria in a 27-week fetus: An architectonic and topographic analysis . J Neuropathol Exp Neurol1974;33:374-384.
18.
Williams RS, Ferrante RJ, Caviness VS: The cellular pathology of microgyria. Acta Neuropathol (Berl) 1976;36:269-283.
19.
Avery ME, Taeusch HW: Stridors in the newborn, in Schaffer's Diseases of the Newborn , 5th ed. Philadelphia , WB Saunders, 1984, pp 122-128.
20.
Colvin EV: Cardiac embryology, in The Science and Practice of Pediatric Cardiology. Philadelphia, Lea & Febiger, 1990, pp 71-108.
21.
Münke M.: Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly. Am J Med Genet1989;34:237-245.
22.
Jacobson M.: The neural crest and its derivatives, in Developmental Neurobiology , 3rd ed. New York , Plenum Press, 1991, pp 143-162.