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	1.	[Risk factors of arteriosclerosis in expert opinion]. [electronic resource] by Bofinger, M Producer: 19740225 In: Zeitschrift fur Allgemeinmedizin vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	2.	Cat eye syndrome. Partial trisomy 22 due to translocation in the mother. [electronic resource] by Bofinger, M K Soukup, S W Producer: 19770929 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)
	3.	Letter: Warfarin and fetal abnormality. [electronic resource] by Bofinger, M K Warkany, J Producer: 19760802 In: Lancet (London, England) vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Median facial cleft syndrome in half-sisters. Dilemmas in genetic counseling. [electronic resource] by Warkany, J Bofinger, M K Benton, C Producer: 19740228 In: Teratology vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Noncompaction of the ventricular myocardium in Melnick-Needles syndrome. [electronic resource] by Wong, J A Bofinger, M K Producer: 19970904 In: American journal of medical genetics vol. 71 Availability: No items available. Save to lists Add to cart (remove)
	6.	Prominent transverse (Bowdler) bone spurs as a diagnostic clue in a case of neonatal hypophosphatasia without metaphyseal irregularity. [electronic resource] by Oestreich, A E Bofinger, M K Producer: 19890828 In: Pediatric radiology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Spontaneous resolution of fetal cystic hygroma and hydrops in Turner syndrome. [electronic resource] by Mostello, D J Bofinger, M K Siddiqi, T A Producer: 19890519 In: Obstetrics and gynecology vol. 73 Availability: No items available. Save to lists Add to cart (remove)
	8.	Pathologic features of the eye in Down's syndrome with relationship to other chromosomal anomalies. [electronic resource] by Ginsberg, J Bofinger, M K Roush, J R Producer: 19770729 In: American journal of ophthalmology vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Ultrasound and genetic features of a term triploid pregnancy. [electronic resource] by Wasserman, S A Bofinger, M K Saldana, L R Producer: 19920622 In: American journal of perinatology vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Galactose-1-phosphate accumulation by a Duarte-transferase deficiency double heterozygote. [electronic resource] by Wharton, C H Berry, H K Bofinger, M K Producer: 19780426 In: Clinical genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Reduction malformations and chromosome anomalies. [electronic resource] by Bofinger, M K Dignan, P S Schmidt, R E Warkany, J Producer: 19730315 In: American journal of diseases of children (1960) vol. 125 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	[Suicide attempt with phentermine]. [electronic resource] by Eberhardt, H Freundt, K J von Clarmann, M Bofinger, M Producer: 19660925 In: Archiv fur Toxikologie vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	13.	Intellectual development and academic achievement of children treated early for phenylketonuria. [electronic resource] by Berry, H K O'Grady, D J Perlmutter, L J Bofinger, M K Producer: 19791024 In: Developmental medicine and child neurology vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Increased need for medical interventions in infants with velocardiofacial (deletion 22q11) syndrome. [electronic resource] by Hopkin, R J Schorry, E K Bofinger, M Saal, H M Producer: 20000919 In: The Journal of pediatrics vol. 137 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Diagnosis of phenylalanine hydroxylase deficiency (phenylketonuria). [electronic resource] by Berry, H K Hsieh, M H Bofinger, M K Schubert, W K Producer: 19820521 In: American journal of diseases of children (1960) vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Strokes, cutis marmorata telangiectatica congenita, and factor V Leiden. [electronic resource] by Gruppo, R A DeGrauw, T J Palasis, S Kalinyak, K A Bofinger, M K Producer: 19980727 In: Pediatric neurology vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Reduction of cerebrospinal fluid phenylalanine after oral administration of valine, isoleucine, and leucine. [electronic resource] by Berry, H K Bofinger, M K Hunt, M M Phillips, P J Guilfoile, M B Producer: 19821216 In: Pediatric research vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	45,X/46,X,r(Y) karyotype transmitted by father to son after intracytoplasmic sperm injection for oligospermia. A case report. [electronic resource] by Bofinger, M K Needham, D F Saldana, L R Sosnowski, J P Blough, R I Producer: 19991021 In: The Journal of reproductive medicine vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	19.	Premature closure of foramen ovale and renal vein thrombosis in a stillborn twin homozygous for methylene tetrahydrofolate reductase gene polymorphism: a clinicopathologic case study. [electronic resource] by Stanek, J Bove, K E Bofinger, M Needham, D Saldana, L R Mutema, G K Meyer, R Producer: 20000608 In: Journal of perinatal medicine vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Comparative diagnostic value of phenylalanine challenge and phenylalanine hydroxylase activity in phenylketonuria. [electronic resource] by Hsieh, M C Berry, H K Bofinger, M K Phillips, P J Guilfoile, M B Hunt, M M Producer: 19831021 In: Clinical genetics vol. 23 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 22 results.