Your search returned 1120 results.

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	121.	[Polycystic renal diseases: morphology and genetic counseling]. [electronic resource] by Moerman, P Fryns, J P Producer: 19850826 In: Journal de genetique humaine vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	122.	Normal/trisomy 13 mosaicism in a 38-year-old male. [electronic resource] by Petit, P Fryns, J P Producer: 19950209 In: Genetic counseling (Geneva, Switzerland) vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	123.	Miller postaxial acrofacial dysostosis. The phenotypic changes with age. [electronic resource] by Chrzanowska, K Fryns, J P Producer: 19930928 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	124.	Malformative syndrome with trigonocephaly, shallow orbits, ptosis, growth and mental retardation. De novo autosomal reciprocal t(9;13)(Q32;Q22) in a male patient. [electronic resource] by Fryns, J P Hendrickx, G Producer: 19970917 In: Annales de genetique vol. 39 Availability: No items available. Save to lists Add to cart (remove)
	125.	Precocious puberty in Klinefelter syndrome: non-specific result of neurological deficit? [electronic resource] by Fryns, J P Devriendt, K Producer: 19971020 In: American journal of medical genetics vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	126.	Trisomy 21 in a second trimester male hydropic fetus with "Noonan-syndrome-phenotype": nuchal and thoracic lymphangiomatosis, oedema of the dorsum of hands and feet, and bicuspid pulmonary valve. [electronic resource] by Fryns, J P Moerman, P Producer: 19980710 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	127.	"Cataplexy" in Coffin-Lowry syndrome. [electronic resource] by Fryns, J P Smeets, E Producer: 19981113 In: Journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	128.	Goeminne syndrome (OMIM 314300): another male patient 30 years later. [electronic resource] by Fryns, J P Gevers, D Producer: 20030827 In: Genetic counseling (Geneva, Switzerland) vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	129.	Scalp defects in Fryns syndrome. [electronic resource] by Fryns, J P Moerman, P Producer: 19980922 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	130.	Short limbed dwarfism, genital hypoplasia, sparse hair, and vertebral anomalies: a variant of Ellis-van Creveld syndrome? [electronic resource] by Fryns, J P Moerman, P Producer: 19930610 In: Journal of medical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	131.	WITHDRAWN: Human chromosome fragility. [electronic resource] by Lukusa, T Fryns, J P Publication details: Biochimica et biophysica acta Oct 2007 In: Biochimica et biophysica acta p. None Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	132.	Oculocerebral syndrome with hypopigmentation (Cross syndrome): the mixed pattern of hair pigmentation as an important diagnostic sign. [electronic resource] by De Jong, G Fryns, J P Producer: 19920424 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	133.	Cowden syndrome. [electronic resource] by Hanssen, A M Fryns, J P Producer: 19950628 In: Journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	134.	Follow-up report on the 'Poland anomaly/primary microcephaly association'. [electronic resource] by Fryns, J P De Smet, L Producer: 19970326 In: Clinical dysmorphology vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	135.	Anal atresia and abdominal wall defect as unusual symptoms in EEC syndrome. [electronic resource] by De Smet, L Fryns, J P Producer: 19951109 In: Genetic counseling (Geneva, Switzerland) vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	136.	Floating-Harbor syndrome in two sisters: autosomal recessive inheritance or germinal mosaicism? [electronic resource] by Ioan, D M Fryns, J P Producer: 20040421 In: Genetic counseling (Geneva, Switzerland) vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	137.	Prader-Willi syndrome: a review with special attention to the cognitive and behavioral profile. [electronic resource] by Curfs, L M Fryns, J P Producer: 19931217 In: Birth defects original article series vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	138.	MASA syndrome. [electronic resource] by Schrander-Stumpel, C Fryns, J P Producer: 19921202 In: Clinical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	139.	Another look at the causes of the windblown hand. [electronic resource] by Fryns, J P De Smet, L Producer: 19951205 In: Journal of hand surgery (Edinburgh, Scotland) vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	140.	MCA/MR syndrome with occipital scalp defect and valvular pulmonary stenosis: a cryptic 7pter duplication/18qter deficiency. [electronic resource] by Fryns, J P de Cock, P Producer: 20010726 In: Genetic counseling (Geneva, Switzerland) vol. 12 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1120 results.