Keyphrases
Coloboma
100%
Intellectual Disability
66%
Growth Retardation
66%
Syndrome Identification
66%
Trigonocephaly
66%
Chromosome 2
50%
Brain Malformation
50%
Intrauterine Growth Retardation
50%
Ptosis
44%
Size at Birth
44%
Skeletal Anomalies
44%
Scoliosis
38%
Behavior Problems
36%
Mouse Genetics
33%
Leukonychia
33%
Palmoplantar Hyperkeratosis
33%
Long Arm
33%
Knuckle Pads
33%
Identical Twins
33%
Malformation
33%
Electron Microscopic
33%
Microscopic Observation
33%
Baraitser-Winter Cerebrofrontofacial Syndrome
33%
Marden-Walker Syndrome
33%
Bone Defect
33%
Sudden Sensorineural Hearing Loss (SSNHL)
33%
Autism
33%
Behavior Modification
33%
Radiological Findings
33%
Wechsler Adult Intelligence Scale
33%
Derivative Chromosome
33%
Limb Malformation
33%
Cardiac Malformation
33%
Genotype-phenotype Correlation
33%
Cerebral Palsy
33%
Phenotypic Spectrum
33%
Physical Findings
33%
Attention Deficit Hyperactivity Disorder
33%
Type I Chiari Malformation
33%
Noonan Syndrome
33%
Syringomyelia
33%
Single-family
33%
Anorexia Nervosa
33%
Hospitalization
33%
Neural Tube Defects
33%
Child Self-report
33%
Microcephaly
33%
Frontal Bone
33%
Open Heart Surgery
33%
Interstitial Deletion
33%
Medicine and Dentistry
Coloboma
77%
Growth Retardation
66%
Congenital Malformation
61%
Brain Malformation
50%
Chromosome 2
50%
Macrogyria
44%
Leukodystrophy
33%
Leukonychia
33%
Palmoplantar Keratoderma
33%
Connective Tissue Disease
33%
Psychomotor Retardation
33%
Blepharophimosis
33%
Bone Defect
33%
Syndrome Delineation
33%
Frontal Bone
33%
Arm
33%
Syringomyelia
33%
Noonan Syndrome
33%
Hyperactivity
33%
Webbed Neck
33%
Body of Vertebra
33%
Actin
33%
Limb Malformation
33%
Axial Skeleton
33%
Rib Malformation
33%
Mandibuloacral Dysplasia
33%
Arnold Chiari Malformation
33%
Ptosis
33%
Karyotype
33%
Spastic Diplegia
33%
Synostosis
33%
Short Stature
33%
Disease
27%
Palpebral Fissure
27%
Microcephaly
27%
Hypertelorism
22%
Midface Hypoplasia
16%
Meningocele
16%
Encephalocele
16%
Chromosome 6
16%
Ventricular Septal Defect
16%
Cardiovascular Malformation
16%
Pericentric Chromosome Inversion
16%
Cleft Palate
16%
Limb Defect
16%
Face Malformation
16%
Premature Aging
16%
Hypohidrotic Ectodermal Dysplasia
16%
Prometaphase
16%
Sensorineural Hearing Loss
11%
