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Differential
(Click to cross reference)
acromicria
aggression
amniocentesis
Angelman syndrome
ataxia
ataxic gait
attention span
behavior, combative
behavioral disorder
brachycephaly
cerebellar atrophy, primary
cerebral cortical atrophy
children
chromosomal abnormality
chromosome 15
corpus callosum
corpus callosum, atrophy of
corpus callosum, thinning
cry, abnormal
cry, weak
developmental retardation
drooling
dural ectasia
dysmorphic
ears of the Lynx MR sign
eating disorder
electroencephalogram, abnormalities of
facial appearance, abnormal
facial expression abnormality
failure to thrive
feeding disorder
fish
fluorescene in situ hybridization
gait disorder
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
growth hormone deficiency
hand flapping
hyperactivity
hyperphagia
hypogonadism
hypopigmentation of skin
hypotonia
hypotonia, infants
imbalance
intellectual deficit
laughing, pathologic
macrognathia
Marfan syndrome
mental retardation
microcephaly
misdiagnosis
molecular genetics
MRI, abnormal
MRI, spine
neurologic disease, diagnoses of
obesity
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
postural abnormality
Prader-Labhart-Willi syndrome
prenatal diagnosis by amniocentesis
prognathism
review article
seizure
short stature
smiling
spastic paraplegia, type 11
spastic paraplegia, type 15
speech disorder
speech disorder, childhood
speech, delayed development of
strabismus
suck, poor
teeth, wide-spaced
temper tantrums
tongue, protrusion of
tremulousness
vertebral scalloping
wide based gait
Showing articles 1300 to 1324 of 1324 << Previous

Pediatric Neurology
Psych Annals 2:1, , 1972

Ethical & Social Issues in Screening for Genetic Disease-Screening for Genetic Disease-A Group Report
NEJM 286:1129, 1972, 286:1155972., , 1972

Maternal Epilepsy & Abnormalities of the Fetus & Newborn
Lancet 839, Oct1972., Speidel,B.,et al, 1972

Presymptomatic Detection of Huntington's Chorea
BMJ 540, 1972 Sept., , 1972

Machado Disease-a Hereditary Ataxia in Portuguese Emigrants to Mass
Neurol 22:49, Nakano,K.K.,et al, 1972

Preclinical Detection of Dystrophia Myotonica
BMJ 124, 1972 April., , 1972

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
(Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972

Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue
(Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972

The Mucopolysaccharidoses
(Ed) , 4th Edition, the C. V. Mosby Co, 1971, Chp. 11, p. p. 521-686., McKusick,V.A., 1971

Dominant Juvenile Optic Atrophy
Arch Ophthalmol 85:133, Caldwell,J.,et al, 1971

Prenatal Genetic Diagnosis
NEJM 283:1370, Milunsky,A.,et al, 1970

Hunter's Syndrome, In Recognizable Patterns Of Human Malformation, Genetic, Embryologic, & Clinical Aspects, by Smith
W. B. , Saunders Co. , 1970, 248-249., David,W., 1970

Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969

The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,et al, 1968

Myopathy of the Quadriceps Muscles
J Neurol Sci 7:201, VanWijngaarden,G.K.,et al, 1968

Spastic Pseudosclerosis (Creutzfeldt-Jakob Dis) Van Rossum A. , In:Vinken, P. J.
Handbk of Clin Neurol Vol 6 North-Holland Publ. Amster 1968 Ch 28, p 726., Bruyn,G.W., 1968

Huntington's Chorea
Bruyn, G. W. In Vinken & Bruyn, Handbk of Clin Neurol, North-Holland Publ Co, Amsterdam, 6:298, , 1968

Screening for Inborn Errors of Metabolism Associated with Mental Deficiency or Neurologic Disorders or Both
NEJM 274:384, Renuart,A., 1966

Inherited Aminoacidopathies Demonstrating Vitamin Dependency
NEJM 281:145, Rosenberg,L., 1965

Morquio's Disease, A Radiologic & Morphologic Study
Pediatrics 34:839-850, Schenk,E.A.&Haggerty,J., 1964

Familial and Conjugal Multiple Sclerosis
Brain 86:315-332, Schapira,K.,et al, 1963

The Cornelia de Lange Syndrome
J Pediatr 63:1000-1020, Ptacek,L.J., 1963

Angiokeratoma Corporis Diffusum
Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962

Microcephaly
Arch Dis Child 37:623-627, Davies,H.,et al, 1962

Clinical Study of Nine Patients with ReNU Syndrome
, Okamoto,N.,et al,



Showing articles 1300 to 1324 of 1324 << Previous