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	1.	Chromosome abnormality in an isolated choroid plexus cyst. [electronic resource] by Suslak, L Pletcher, B A Producer: 19950714 In: Prenatal diagnosis vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Osteogenesis imperfecta with joint contractures: bruck syndrome. [electronic resource] by Blacksin, M F Pletcher, B A David, M Producer: 19980409 In: Pediatric radiology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A PPY cDNA clone identifies a frequent RFLP. [electronic resource] by Pletcher, B A Takeuchi, T Kidd, J R Producer: 19871118 In: Nucleic acids research vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Congenital bifid sternum: repair in early infancy and literature review. [electronic resource] by Greenberg, B M Becker, J M Pletcher, B A Producer: 19911121 In: Plastic and reconstructive surgery vol. 88 Availability: No items available. Save to lists Add to cart (remove)
	5.	Anterior polar cataract in two sisters with an unbalanced 3;18 chromosomal translocation. [electronic resource] by Rubin, S E Nelson, L B Pletcher, B A Producer: 19940509 In: American journal of ophthalmology vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Interstitial duplication of proximal 22q: phenotypic overlap with cat eye syndrome. [electronic resource] by Knoll, J H Asamoah, A Pletcher, B A Wagstaff, J Producer: 19950512 In: American journal of medical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Familial occurrence of esophageal atresia with and without tracheoesophagel fistula: report of two unusual kindreds. [electronic resource] by Pletcher, B A Friedes, J S Breg, W R Touloukian, R J Producer: 19910923 In: American journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	NF1 microdeletion breakpoints are clustered at flanking repetitive sequences. [electronic resource] by Dorschner, M O Sybert, V P Weaver, M Pletcher, B A Stephens, K Producer: 20000229 In: Human molecular genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Filippi syndrome: report of three additional cases. [electronic resource] by Williams, M S Williams, J L Wargowski, D S Pauli, R M Pletcher, B A Producer: 19991130 In: American journal of medical genetics vol. 87 Availability: No items available. Save to lists Add to cart (remove)
	10.	Intrauterine cytomegalovirus infection presenting as fetal meconium peritonitis. [electronic resource] by Pletcher, B A Williams, M K Mulivor, R A Barth, D Linder, C Rawlinson, K Producer: 19911121 In: Obstetrics and gynecology vol. 78 Availability: No items available. Save to lists Add to cart (remove)
	11.	Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC). [electronic resource] by Rosenblatt, D S Aspler, A L Shevell, M I Pletcher, B A Fenton, W A Seashore, M R Producer: 19971014 In: Journal of inherited metabolic disease vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Searching for a major genetic locus for affective disorder in the Old Order Amish. [electronic resource] by Kidd, J R Egeland, J A Pakstis, A J Castiglione, C M Pletcher, B A Morton, L A Kidd, K K Producer: 19880408 In: Journal of psychiatric research vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Four sibs with arterial tortuosity: description and review of the literature. [electronic resource] by Pletcher, B A Fox, J E Boxer, R A Singh, S Blumenthal, D Cohen, T Brunson, S Tafreshi, P Kahn, E Producer: 19970225 In: American journal of medical genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	One large kindred excludes a locus for multiple endocrine neoplasia type 2A from about 25% of the human autosomal genetic map. [electronic resource] by Pakstis, A J Kidd, J R Castiglione, C M Pletcher, B A Murphy, P D Farrer, L A Genel, M Kidd, K K Producer: 19880225 In: Henry Ford Hospital medical journal vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	15.	Postnatal confirmation of prenatally diagnosed trisomy 16 mosaicism in two phenotypically abnormal liveborns. [electronic resource] by Pletcher, B A Sanz, M M Schlessel, J S Kunaporn, S McKenna, C Bialer, M G Alonso, M L Zaslav, A L Brown, W T Ray, J H Producer: 19950427 In: Prenatal diagnosis vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Inherited duplication Xq27-qter at Xp22.3 in severely affected males: molecular cytogenetic evaluation and clinical description in three unrelated families. [electronic resource] by Goodman, B K Shaffer, L G Rutberg, J Leppert, M Harum, K Gagos, S Ray, J H Bialer, M G Zhou, X Pletcher, B A Shapira, S K Geraghty, M T Producer: 19990217 In: American journal of medical genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)