Topic: Child
Journal: American Journal of Medical Genetics. Part A
Documents
A list of abstracts that contain a topic of "Child" and a journal name of "American Journal of Medical Genetics. Part A".
Periventricular Nodular Heterotopia and Williams Syndrome.
PMID: 16691586
Single Maxillary Central Incisor, Holoprosencephaly, and Holoprosencephaly-like Phenotype.
PMID: 17001670
Is There a Higher Incidence of Maternal Uniparental Disomy 14 [Upd(14)mat]? Detection of 10 New Patients by Methylation-specific Pcr.
PMID: 16906536
Overgrowth with Severe Developmental Delay Following Ivf/Icsi: A Newly Recognized Syndrome?
PMID: 16691625
Thyroid Anomalies in Williams Syndrome: Investigation of 95 Patients.
PMID: 16596673
Smith-magenis Syndrome and Moyamoya Disease in a Patient with Del(17)(P11.2p13.1).
PMID: 17431895
A Study of Familial Stuttering.
PMID: 16752384
Microdeletion and Microduplication 22q11.2 Screening in 295 Patients with Clinical Features of Digeorge/Velocardiofacial Syndrome.
PMID: 17041934
Identification of Novel Mutations in Wfs1 and Genotype-phenotype Correlation in Wolfram Syndrome.
PMID: 17568405
Dural Ectasia in Children with Marfan Syndrome: a Prospective, Multicenter, Patient-control Study.
PMID: 16523504