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	1.	Aplasia cutis congenita, terminal limb defects and periventricular leukomalacia in one sibling with minor findings in the other-probable autosomal recessive Adams-Oliver Syndrome. [electronic resource] by Balasubramanian, Meena Collins, Amanda L Producer: 20091102 In: European journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Zimmermann-Laband syndrome in a child previously described with brachydactyly, extrahepatic biliary atresia, patent ductus arteriosus and seizures. [electronic resource] by Balasubramanian, Meena Parker, Michael J Producer: 20100222 In: Clinical dysmorphology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Short sternum: feature of trisomy chromosome 7 and a new association? [electronic resource] by Balasubramanian, Meena Peres, Luiz Cesar Producer: 20140515 In: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	MAN1B-CDG: Novel variants with a distinct phenotype and review of literature. [electronic resource] by Balasubramanian, Meena Johnson, Diana S Producer: 20190305 In: European journal of medical genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	De novo SETD5 loss-of-function variant as a cause for intellectual disability in a 10-year old boy with an aberrant blind ending bronchus. [electronic resource] by Green, Claire Willoughby, Joshua Balasubramanian, Meena Producer: 20180321 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)
	6.	Inherited duplication of the short arm of chromosome 18p11.32-p11.31 associated with developmental delay/intellectual disability. [electronic resource] by Balasubramanian, Meena Sithambaram, Sivagamy Smith, Kath Producer: 20160928 In: Clinical dysmorphology vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	SHANK3 variant as a cause of nonsyndromal autism in an 11-year-old boy and a review of published literature. [electronic resource] by Kanani, Farah Study, Ddd Balasubramanian, Meena Producer: 20181025 In: Clinical dysmorphology vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Compound heterozygous variants in IFT140 as a cause of nonsyndromic retinitis pigmentosa. [electronic resource] by Low, Tisiana Kostakis, Anastassios Balasubramanian, Meena Producer: 20190311 In: Ophthalmic genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Congenital myotonic dystrophy: natural disease progression and facial dysmorphology. [electronic resource] by Balasubramanian, Meena Sayers, Richard Martindale, Joanne Producer: 20150831 In: Clinical dysmorphology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Clinical and molecular characterization of the first familial report of 1p32 microdeletion. [electronic resource] by Schirwani, Schaida Smith, Kath Balasubramanian, Meena Producer: 20180903 In: Clinical dysmorphology vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Short case report: Xq23 deletion involving PAK3 as a novel cause of developmental delay in a 6-year-old boy. [electronic resource] by Cartwright, Ashley Smith, Kath Balasubramanian, Meena Producer: 20170206 In: Clinical dysmorphology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Mosaic trisomy 11 in a fetus with bilateral renal agenesis: co-incidence or new association? [electronic resource] by Balasubramanian, Meena Peres, Luiz Cesar Pelly, Dorothy Producer: 20110316 In: Clinical dysmorphology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	IMAGe syndrome: Case report with a previously unreported feature and review of published literature. [electronic resource] by Balasubramanian, Meena Sprigg, Alan Johnson, Diana S Producer: 20110315 In: American journal of medical genetics. Part A vol. 152A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Clinical report: inherited deletion of chromosome 12q21.31q21.32 associated with a distinct phenotype and intellectual disability. [electronic resource] by Akilapa, Rhoda S Smith, Kath Balasubramanian, Meena Producer: 20160620 In: Clinical dysmorphology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Exploring the association between SRPX2 variants and neurodevelopment: How causal is it? [electronic resource] by Schirwani, Schaida McConnell, Vivienne Willoughby, Josh Balasubramanian, Meena Producer: 20190101 In: Gene vol. 685 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Atypical, milder presentation in a child with CC2D2A and KIDINS220 variants. [electronic resource] by Lam, Zena Albaba, Shadi Study, Ddd Balasubramanian, Meena Producer: 20200416 In: Clinical dysmorphology vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Expanding the molecular basis and phenotypic spectrum of ZDHHC9-associated X-linked intellectual disability. [electronic resource] by Schirwani, Schaida Wakeling, Emma Smith, Kath Balasubramanian, Meena Producer: 20190520 In: American journal of medical genetics. Part A vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	A novel de novo 20q13.32-q13.33 deletion in a 2-year-old child with poor growth, feeding difficulties and low bone mass. [electronic resource] by Balasubramanian, Meena Atack, Edward Smith, Kath Parker, Michael James Producer: 20160229 In: Journal of human genetics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Dual diagnosis causing severe phenotype in a patient with Angelman syndrome. [electronic resource] by Kanani, Farah Mordekar, Santosh Parker, Michael J Balasubramanian, Meena Producer: 20191206 In: Clinical dysmorphology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Osteogenesis imperfecta type 1 with an incidental finding of bilateral radioulnar synostosis. [electronic resource] by Apperley, Louise J Richmond, Stacey Ramakrishnan, Renuka Balasubramanian, Meena Producer: 20210504 In: Clinical dysmorphology vol. 29 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 61 results.