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	1.	Trisomy 8 mosaicism and favorable outcome after treatment of infantile spasms: case report. [electronic resource] by Datta, Anita Picker, Jonathan Rotenberg, Alexander Producer: 20110815 In: Journal of child neurology vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Do maternal folate and homocysteine levels play a role in neurodevelopmental processes that increase risk for schizophrenia? [electronic resource] by Picker, Jonathan D Coyle, Joseph T Producer: 20060103 In: Harvard review of psychiatry vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	New innovations: therapeutic opportunities for intellectual disabilities. [electronic resource] by Picker, Jonathan D Walsh, Christopher A Producer: 20131210 In: Annals of neurology vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Utility of Genetic Testing in Fetal Alcohol Spectrum Disorder. [electronic resource] by Jamuar, Saumya S Picker, Jonathan D Stoler, Joan M Producer: 20190225 In: The Journal of pediatrics vol. 196 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Review of Salient Investigational Drugs for the Treatment of Fragile X Syndrome. [electronic resource] by Munshi, Kaizad Pawlowski, Katherine Gonzalez-Heydrich, Joseph Picker, Jonathan D Producer: 20180719 In: Journal of child and adolescent psychopharmacology vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Peri-mortem evaluation of infants who die without a diagnosis: focus on advances in genomic technology. [electronic resource] by Wojcik, Monica H Brodsky, Dara Stewart, Jane E Picker, Jonathan Producer: 20191111 In: Journal of perinatology : official journal of the California Perinatal Association vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	An altered neonatal behavioral phenotype in Mecp2 mutant mice. [electronic resource] by Picker, Jonathan D Yang, Rebecca Ricceri, Laura Berger-Sweeney, Joanne Producer: 20060517 In: Neuroreport vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Familial deletion within NLGN4 associated with autism and Tourette syndrome. [electronic resource] by Lawson-Yuen, Amy Saldivar, Juan-Sebastian Sommer, Steve Picker, Jonathan Producer: 20080612 In: European journal of human genetics : EJHG vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Neonatal screening for medium--chain acyl-CoA dehydrogenase deficiency. [electronic resource] by Fowler, Darren J Picker, Jonathan Waisbren, Susan E Levy, Harvey L Producer: 20020305 In: Lancet (London, England) vol. 359 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Smith-Lemli-Opitz syndrome in trisomy 13: how does the mix work? [electronic resource] by Alkuraya, Fowzan S Picker, Jonathan Irons, Mira B Kimonis, Virginia E Producer: 20051201 In: Birth defects research. Part A, Clinical and molecular teratology vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	None [electronic resource] by Kim, Hyun Chadwick, Laura Alzaidi, Yasir Picker, Jonathan Poduri, Annapurna Manzi, Shannon Producer: 20190503 In: Pediatrics vol. 141 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Revising the Psychiatric Phenotype of Homocystinuria. [electronic resource] by Almuqbil, Mohamed A Waisbren, Susan E Levy, Harvey L Picker, Jonathan D Producer: 20200206 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Delayed puberty due to a novel mutation in CHD7 causing CHARGE syndrome. [electronic resource] by Dauber, Andrew Hirschhorn, Joel N Picker, Jonathan Maher, Thomas A Milunsky, Aubrey Producer: 20110208 In: Pediatrics vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	EEG abnormalities and seizures in genetically diagnosed Fragile X syndrome. [electronic resource] by Heard, Takijah T Ramgopal, Sriram Picker, Jonathan Lincoln, Sharyn A Rotenberg, Alexander Kothare, Sanjeev V Producer: 20150821 In: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Response to: Toriello et al., "Update on the Toriello-Carey Syndrome." Further delineation of a young woman with deletion 1q42.12-q42.2. [electronic resource] by Garza-Flores, Alexandra Hawley, Pamela Picker, Jonathan Tannebring, Elizabeth Deardorff, Matthew A Lin, Angela E Publication details: American journal of medical genetics. Part A Jul 2017 In: American journal of medical genetics. Part A vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Compound heterozygosity of predicted loss-of-function DES variants in a family with recessive desminopathy. [electronic resource] by McLaughlin, Heather M Kelly, Melissa A Hawley, Pamela P Darras, Basil T Funke, Birgit Picker, Jonathan Producer: 20130826 In: BMC medical genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin gene. [electronic resource] by Rodan, Lance H Cohen, Julie Fatemi, Ali Gillis, Tammy Lucente, Diane Gusella, James Picker, Jonathan D Publication details: European journal of human genetics : EJHG 12 2016 In: European journal of human genetics : EJHG vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin gene. [electronic resource] by Rodan, Lance H Cohen, Julie Fatemi, Ali Gillis, Tammy Lucente, Diane Gusella, James Picker, Jonathan D Producer: 20170711 In: European journal of human genetics : EJHG vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Multicolor karyotypic interpretation of a heterochromatin-associated marker chromosome in a dysmorphic girl with developmental delay. [electronic resource] by Picker, Jonathan D Cox, Gerry F Fan, Yao-Shan Fowler, Darren J Weremowicz, Stanislawa Morton, Cynthia C Lee, Charles Producer: 20021025 In: American journal of medical genetics vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Abnormal Mechanisms of Plasticity and Metaplasticity in Autism Spectrum Disorders and Fragile X Syndrome. [electronic resource] by Oberman, Lindsay M Ifert-Miller, Fritz Najib, Umer Bashir, Shahid Heydrich, Joseph Gonzalez Picker, Jonathan Rotenberg, Alexander Pascual-Leone, Alvaro Producer: 20180119 In: Journal of child and adolescent psychopharmacology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 48 results.