Arch Pediatr Adolesc Med -- Table of Contents (Vol. 147 No. 11, November 1993)

You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.

Table of Contents

ARTICLES

Genetics: the quiet revolution in science and medicine. Implications for research on child health issues, education of health professionals, and the new preventive and curative medicine
V. A. Fulginiti
Am J Dis Child. 1993;147:1139-1141.

The Human Genome Project and the future of medicine
M. S. Guyer; F. S. Collins
Am J Dis Child. 1993;147:1145-1152.
ABSTRACT

State of the art of biochemical genetics
P. Levy; E. Shapira
Am J Dis Child. 1993;147:1153-1158.

Human cytogenetics. A current overview
M. M. Cohen; L. S. Rosenblum-Vos; G. Prabhakar
Am J Dis Child. 1993;147:1159-1166.
ABSTRACT

Gene therapy
F. Levine; T. Friedmann
Am J Dis Child. 1993;147:1167-1174.

Modern diagnosis and treatment of Gaucher's disease
E. Beutler
Am J Dis Child. 1993;147:1175-1183.

The state of the art of dysmorphology
B. D. Hall
Am J Dis Child. 1993;147:1184-1189.
ABSTRACT

Genetic diagnosis and treatment. Ethical considerations
N. Fost
Am J Dis Child. 1993;147:1190-1195.

Telediagnostic conferencing
M. Feingold; J. Frias; A. E. Lin; G. B. Schaefer; M. Horwitz
Am J Dis Child. 1993;147:1196.

Sickle cell anemia. Beta s gene cluster haplotypes as genetic markers for severe disease expression
D. Powars; A. Hiti
Am J Dis Child. 1993;147:1197-1202.
ABSTRACT

The genetics of infantile hypertrophic pyloric stenosis. A reanalysis
L. E. Mitchell; N. Risch
Am J Dis Child. 1993;147:1203-1211.
ABSTRACT

Velo-cardio-facial syndrome. Intrafamilial variability of the phenotype
S. D. McLean; H. M. Saal; N. B. Spinner; B. S. Emanuel; D. A. Driscoll
Am J Dis Child. 1993;147:1212-1216.
ABSTRACT

Clinical correlates of chromosome 15 deletions and maternal disomy in Prader-Willi syndrome
L. W. Lai; R. P. Erickson; S. B. Cassidy
Am J Dis Child. 1993;147:1217-1223.
ABSTRACT

The North American Collaborative Study of Maternal Phenylketonuria. Status report 1993
R. Koch; H. L. Levy; R. Matalon; B. Rouse; W. Hanley; C. Azen
Am J Dis Child. 1993;147:1224-1230.
ABSTRACT

Direct DNA testing for fragile X syndrome
F. J. Ramos; D. L. Eunpu; B. Finucane; E. G. Pfendner
Am J Dis Child. 1993;147:1231-1235.
ABSTRACT

A study of the physical, behavioral, and medical phenotype, including anthropometric measures, of females with fragile X syndrome
C. Hull; R. J. Hagerman
Am J Dis Child. 1993;147:1236-1241.
ABSTRACT

X-linked lymphoproliferative disease
T. A. Seemayer; H. Grierson; S. J. Pirruccello; T. G. Gross; D. D. Weisenburger; J. Davis; K. Spiegel; B. Brichacek; J. Sumegi
Am J Dis Child. 1993;147:1242-1245.

Williams syndrome, Down syndrome, and cognitive neuroscience
P. P. Wang; U. Bellugi
Am J Dis Child. 1993;147:1246-1251.

Pitfalls in genetic counseling for childhood disorders: the pediatrician's role
L. R. Shapiro
Am J Dis Child. 1993;147:1253-1254.

Acute lymphoblastic leukemia in a 46,XY/47,XYY mosaic male: clonal origin of leukemia in the XY-bearing stem-cell line
J. W. Taub; Y. Ravindranath; A. N. Mohamed; S. R. Wolman; E. V. Bawle
Am J Dis Child. 1993;147:1254-1255.