Your search returned 78 results.

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	1.	Genetic diagnosis in the newborn. A part of preventive medicine. [electronic resource] by Hecht, F Lovrien, E W Producer: 19710113 In: Pediatric clinics of North America vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Management of fractures in hemophilia. [electronic resource] by Wolff, L J Lovrien, E W Producer: 19821012 In: Pediatrics vol. 70 Availability: No items available. Save to lists Add to cart (remove)
	3.	Haemopexin in human serum: a search for genetic polymorphosm. [electronic resource] by Stewart, R E Lovrien, E W Producer: 19711117 In: Annals of human genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Oral motor dysfunction in individuals at risk of Huntington disease. [electronic resource] by Coleman, R Anderson, D Lovrien, E Producer: 19901205 In: American journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Chorioangioma of the placenta and intrauterine growth failure. [electronic resource] by King, C R Lovrien, E W Producer: 19790212 In: The Journal of pediatrics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Dyschondrosteosis and Madelung's deformity. Report of three kindreds and review of the literature. [electronic resource] by Beals, R K Lovrien, E W Producer: 19760823 In: Clinical orthopaedics and related research no. 116 Availability: No items available. Save to lists Add to cart (remove)
	7.	Diffuse capillary hemangiomas associated with skeletal hypotrophy. [electronic resource] by Beals, R K Lovrien, E W Producer: 19920604 In: Journal of pediatric orthopedics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	GRAND ROUNDS: HASHIMOTO'S THYROIDITIS. [electronic resource] by HUNG, W WINSHIP, T LOVRIEN, E Producer: 19961201 In: Clinical proceedings - Children's Hospital of the District of Columbia vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	9.	Alpha-1-antitrypsin protease inhibitor (Pi) phenotypes in Down's syndrome patients and their parents. [electronic resource] by Bufton, L Magenis, R E Lovrien, E W Producer: 19820624 In: Clinical genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Hereditary melanoma, the dysplastic nevus syndrome, and transferrin. [electronic resource] by Bale, S J Greene, M H Lovrien, E Producer: 19861203 In: Cancer genetics and cytogenetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in man. [electronic resource] by Magenis, R E Hecht, F Lovrien, E W Producer: 19701008 In: Science (New York, N.Y.) vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Central nervous system arteriovenous malformations in multiple generations of a family with hereditary hemorrhagic telangiectasia. [electronic resource] by King, C R Lovrien, E W Reiss, J Producer: 19780223 In: Clinical genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	A mother with Down's syndrome and her chromosomally normal infant. [electronic resource] by Reiss, J A Lovrien, E W Hecht, F Producer: 19711215 In: Annales de genetique vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	14.	Aicardi's syndrome. Case report, clinical features, and electrophysiologic studies. [electronic resource] by Weleber, R G Lovrien, E W Isom, J B Producer: 19780426 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Human chromosome variation: the discriminatory power of Q-band heteromorphism (variant) analysis in distinguishing between individuals, with specific application to cases of questionable paternity. [electronic resource] by Olson, S B Magenis, R E Lovrien, E W Producer: 19860321 In: American journal of human genetics vol. 38 Availability: No items available. Save to lists Add to cart (remove)
	16.	Linkage relationships of HLA and a familial chromosome 6 inversion (pter leads to p23::q23 leads to qter): lack of dose effect in duplication-deficient offspring. [electronic resource] by Magenis, R E Chamberlin, J Overton, K Lovrien, E Producer: 19790925 In: Cytogenetics and cell genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Juvenile sex-linked retinoschisis: clinical and genetic studies. [electronic resource] by Burns, R P Lovrien, E W Cibis, A B Producer: 19711208 In: Transactions - American Academy of Ophthalmology and Otolaryngology. American Academy of Ophthalmology and Otolaryngology vol. 75 Availability: No items available. Save to lists Add to cart (remove)
	18.	Probable genetic linkage between human serum amylase (Amy 2 ) and Duffy blood group. [electronic resource] by Hill, C J Rowe, S I Lovrien, E W Producer: 19720501 In: Nature vol. 235 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	The fetal trimethadione syndrome: report of an additional family and further delineation of this syndrome. [electronic resource] by Feldman, G L Weaver, D D Lovrien, E W Producer: 19780127 In: American journal of diseases of children (1960) vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Unusual dental findings in a patient with a rare bone dysplasia (dyschondrosteosis) and a chromosomal anomaly. [electronic resource] by Stewart, R E Lovrien, E W Wyandt, H E Producer: 19711117 In: Oral surgery, oral medicine, and oral pathology vol. 32 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 78 results.