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Physician collaboration involving students with Autism Spectrum Disorders.
- Published in:
- Psychology in the Schools, 2007, v. 44, n. 7, p. 737, doi. 10.1002/pits.20262
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- Publication type:
- Article
Regulation of MMP-9 (92 kDa type IV collagenase/gelatinase B) expression in stromal cells of human giant cell tumor of bone.
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- Clinical & Experimental Metastasis, 1997, v. 15, n. 4, p. 400, doi. 10.1023/A:1018450204980
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- Publication type:
- Article
Idiopathic Hypothalamic Dysfunction with Precocious Puberty and Adipsic Hypernatremia First Presenting in Adolescence.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2001, v. 14, n. 8, p. 1163, doi. 10.1515/jpem-2001-0816
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- Publication type:
- Article
Cleft Lip and Palate: Association with Other Congenital Malformations.
- Published in:
- Journal of Clinical Pediatric Dentistry, 2009, v. 33, n. 3, p. 207, doi. 10.17796/jcpd.33.3.c244761467507721
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- Publication type:
- Article
Cleft lip and palate: association with other congenital malformations.
- Published in:
- 2009
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- Publication type:
- journal article
Turner syndrome.
- Published in:
- ENT: Ear, Nose & Throat Journal, 1998, v. 77, n. 10, p. 812, doi. 10.1177/014556139807701006
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- Publication type:
- Article
Kabuki Syndrome.
- Published in:
- ENT: Ear, Nose & Throat Journal, 1998, v. 77, n. 9, p. 734, doi. 10.1177/014556139807700909
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- Publication type:
- Article
Oto-palatal-digital syndromes.
- Published in:
- ENT: Ear, Nose & Throat Journal, 1998, v. 77, n. 8, p. 586, doi. 10.1177/014556139807700806
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- Publication type:
- Article
Craniofrontonasal Dysplasia.
- Published in:
- ENT: Ear, Nose & Throat Journal, 1998, v. 77, n. 2, p. 90, doi. 10.1177/014556139807700205
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- Publication type:
- Article
Oculo-auriculo-vertebral spectrum.
- Published in:
- ENT: Ear, Nose & Throat Journal, 1998, v. 77, n. 1, p. 17, doi. 10.1177/014556139807700105
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- Publication type:
- Article
Van der Woude syndrome.
- Published in:
- ENT: Ear, Nose & Throat Journal, 1997, v. 76, n. 12, p. 852, doi. 10.1177/014556139707601204
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- Publication type:
- Article
Oral-Facial-Digital Syndrome Type I.
- Published in:
- ENT: Ear, Nose & Throat Journal, 1997, v. 76, n. 11, p. 778, doi. 10.1177/014556139707601104
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- Publication type:
- Article
Stickler syndrome.
- Published in:
- ENT: Ear, Nose & Throat Journal, 1997, v. 76, n. 10, p. 706, doi. 10.1177/014556139707601005
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- Publication type:
- Article
Correspondence.
- Published in:
- Journal of Child Neurology, 1991, v. 6, n. 4, p. 372, doi. 10.1177/088307389100600414
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- Publication type:
- Article
Age-Related Changes in the Relative Growth of the Posterior Fossa.
- Published in:
- Journal of Child Neurology, 1991, v. 6, n. 1, p. 15, doi. 10.1177/088307389100600103
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- Publication type:
- Article
Hypoplastic Corpus Callosum in Ocular Albinism: Indication of a Global Disturbance of Neuronal Migration.
- Published in:
- Journal of Child Neurology, 1990, v. 5, n. 4, p. 341, doi. 10.1177/088307389000500415
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- Publication type:
- Article
Neuroimaging Findings in Alexander's Disease.
- Published in:
- Journal of Child Neurology, 1990, v. 5, n. 3, p. 253, doi. 10.1177/088307389000500321
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- Publication type:
- Article
Quantitative Morphometric Analysis of Brain Growth Using Magnetic Resonance Imaging.
- Published in:
- Journal of Child Neurology, 1990, v. 5, n. 2, p. 127, doi. 10.1177/088307389000500211
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- Publication type:
- Article
Clinical Genetic Aspects of ASD Spectrum Disorders.
- Published in:
- International Journal of Molecular Sciences, 2016, v. 17, n. 2, p. 180, doi. 10.3390/ijms17020180
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- Publication type:
- Article
Incidental pineal cysts in a prospectively ascertained normal cohort.
- Published in:
- Clinical Pediatrics, 1996, v. 35, n. 5, p. 277, doi. 10.1177/000992289603500510
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- Publication type:
- Article
Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 7, p. 754, doi. 10.1038/ejhg.2012.6
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- Publication type:
- Article
Multi-Tiered Analysis of Brain Injury in Neonates With Congenital Heart Disease.
- Published in:
- Pediatric Cardiology, 2013, v. 34, n. 8, p. 1772, doi. 10.1007/s00246-013-0712-6
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- Publication type:
- Article
Radioulnar Synostosis and Brain Abnormalities in a Patient With 17q21.31 Microdeletion Involving EFTUD2.
- Published in:
- Cleft Palate Craniofacial Journal, 2015, v. 52, n. 2, p. 237, doi. 10.1597/13-221
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- Publication type:
- Article
Persistent congenital hyperinsulinism in two patients with Beckwith-Wiedemann syndrome due to mosaic uniparental disomy 11p.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 951, doi. 10.1515/jpem-2013-0484
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- Publication type:
- Article
Whole exome sequencing reveals EP300 mutation in mildly affected female: expansion of the spectrum.
- Published in:
- Clinical Case Reports, 2016, v. 4, n. 7, p. 696, doi. 10.1002/ccr3.598
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- Publication type:
- Article
The natural history of OTOF-related auditory neuropathy spectrum disorders: a multicenter study.
- Published in:
- Human Genetics, 2022, v. 141, n. 3/4, p. 853, doi. 10.1007/s00439-021-02340-w
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- Publication type:
- Article
Pathogenic in-Frame Variants in SCN8A : Expanding the Genetic Landscape of SCN8A- Associated Disease.
- Published in:
- Frontiers in Pharmacology, 2021, v. 12, p. 1, doi. 10.3389/fphar.2021.748415
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- Publication type:
- Article
Knowledge and Beliefs About Genetics and Smoking Among Visitors and Staff at a Health Care Facility.
- Published in:
- Public Health Nursing, 2008, v. 25, n. 1, p. 77, doi. 10.1111/j.1525-1446.2008.00682.x
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- Publication type:
- Article
Subtle anomalies of the septum pellucidum and neurodevelopmental deficits.
- Published in:
- 1994
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- Publication type:
- journal article
Identification of three novel mutations in human EYA1 protein associated with branchio-oto-renal syndrome.
- Published in:
- Human Mutation, 1998, v. 11, n. 6, p. 443, doi. 10.1002/(SICI)1098-1004(1998)11:6<443::AID-HUMU4>3.0.CO;2-S
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- Publication type:
- Article
Mutation analysis and haplotype correlation for 139 cystic fibrosis patients from the Nebraska Regional Cystic Fibrosis Center.
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- Human Mutation, 1993, v. 2, n. 1, p. 7, doi. 10.1002/humu.1380020103
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- Publication type:
- Article
Identification of DCAF1 by Clinical Exome Sequencing and Methylation Analysis as a Candidate Gene for Autism and Intellectual Disability: A Case Report.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 6, p. 886, doi. 10.3390/jpm12060886
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- Publication type:
- Article
Multidisciplinary Consulting Team for Complicated Cases of Neurodevelopmental and Neurobehavioral Disorders: Assessing the Opportunities and Challenges of Integrating Pharmacogenomics into a Team Setting.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 4, p. 599, doi. 10.3390/jpm12040599
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- Publication type:
- Article
Molecular Dysregulation in Autism Spectrum Disorder.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 9, p. 848, doi. 10.3390/jpm11090848
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- Publication type:
- Article
Implementing Pharmacogenomics Testing: Single Center Experience at Arkansas Children's Hospital.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 5, p. 394, doi. 10.3390/jpm11050394
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- Publication type:
- Article
Quantitation of fibrillin immunofluorescence in fibroblast cultures in the Marfan syndrome.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 3, p. 144, doi. 10.1111/j.1399-0004.1995.tb03947.x
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- Publication type:
- Article
In memory of Murray Feingold (1930-2015).
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 7, p. 1727, doi. 10.1002/ajmg.a.37729
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- Publication type:
- Article
Myhre Syndrome: Clinical Features and Restrictive Cardiopulmonary Complications.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 2893, doi. 10.1002/ajmg.a.37273
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- Publication type:
- Article
Phenotypic modifications of patients with full chromosome aneuploidies and concurrent suspected or confirmed second diagnoses.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 9, p. 2168, doi. 10.1002/ajmg.a.37126
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- Publication type:
- Article
Cardiovascular and genitourinary anomalies in patients with duplications within the Williams syndrome critical region: Phenotypic expansion and review of the literature.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 8, p. 1998, doi. 10.1002/ajmg.a.36601
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- Publication type:
- Article
Characterization of six novel patients with MECP2 duplications due to unbalanced rearrangements of the X chromosome.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 6, p. 1285, doi. 10.1002/ajmg.a.35347
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- Publication type:
- Article
Hypoplasia of the cerebellar vermis in neurogenetic syndromes.
- Published in:
- Annals of Neurology, 1996, v. 39, n. 3, p. 382, doi. 10.1002/ana.410390316
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- Publication type:
- Article
Aplastic Anemia in Two Patients with Sex Chromosome Aneuploidies.
- Published in:
- Cytogenetic & Genome Research, 2016, v. 147, n. 1, p. 31, doi. 10.1159/000441585
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- Publication type:
- Article
Novel de novo EEF1A2 missense mutations causing epilepsy and intellectual disability.
- Published in:
- Molecular Genetics & Genomic Medicine, 2016, v. 4, n. 4, p. 465, doi. 10.1002/mgg3.219
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- Publication type:
- Article
Algorithmic Approach for Methyl-CpG Binding Protein 2 (MECP2) Gene Testing in Patients With Neurodevelopmental Disabilities.
- Published in:
- Journal of Child Neurology, 2012, v. 27, n. 3, p. 346, doi. 10.1177/0883073811424796
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- Publication type:
- Article
Array Comparative Genomic Hybridization Findings in a Cohort Referred for an Autism Evaluation.
- Published in:
- Journal of Child Neurology, 2010, v. 25, n. 12, p. 1498, doi. 10.1177/0883073810370479
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- Publication type:
- Article
Neurocutaneous Disorders.
- Published in:
- 2007
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- Publication type:
- Book Review
Ontogeny and Physiology of the Cavum Septum Pellucidum in Premature Infants.
- Published in:
- Journal of Child Neurology, 2006, v. 21, n. 4, p. 298, doi. 10.1177/08830738060210041501
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- Publication type:
- Article
Hypotonia, Congenital Hearing Loss, and Hypoactive Labyrinths.
- Published in:
- Journal of Child Neurology, 2003, v. 18, n. 3, p. 171, doi. 10.1177/08830738030180030701
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- Publication type:
- Article
Oxford Medical Database (Book).
- Published in:
- 2002
- By:
- Publication type:
- Book Review