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	21.	The fragile X syndrome. A study of 83 families. [electronic resource] by Fryns, J P Producer: 19850122 In: Clinical genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	[Greig's syndrome: variable polysyndactyly associated with distinct craniofacial dymorphism]. [electronic resource] by Fryns, J P Producer: 19830826 In: Journal de genetique humaine vol. 30 Suppl 5 Availability: No items available. Save to lists Add to cart (remove)
	23.	Anophthalmia with cleft palate and micrognathia: a new syndrome or an unusual presentation of Rubinstein-Taybi syndrome? [electronic resource] by Fryns, J P Producer: 19951207 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)
	24.	Micro-ablepharon of the upper eyelids and vaginal atresia. [electronic resource] by Fryns, J P Producer: 20010726 In: Genetic counseling (Geneva, Switzerland) vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	25.	Late-onset isolated cystic hygroma. A first clinical sign of Proteus syndrome. [electronic resource] by Fryns, J P Producer: 19950602 In: Prenatal diagnosis vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Massive hydrocele in postpubertal fra(X) males. [electronic resource] by Fryns, J P Producer: 19940325 In: American journal of medical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Dandy-Walker malformation and postaxial polydactyly: nosological comments. [electronic resource] by Fryns, J P Producer: 19970619 In: Clinical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Ovarian function in fragile X carriers. [electronic resource] by Fryns, J P Producer: 19970318 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	29.	On the nosology of severe acrofacial dysostosis with limb deficiency. [electronic resource] by Fryns, J P Producer: 19990422 In: American journal of medical genetics vol. 82 Availability: No items available. Save to lists Add to cart (remove)
	30.	Structural abnormalities of the Y-chromosome and craniosynostosis. [electronic resource] by 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)
	31.	Chromosomal anomalies and autosomal syndromes. [electronic resource] by Fryns, J P Producer: 19870804 In: Birth defects original article series vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	32.	"Genetic counseling": a "new" discipline with increasing impact on individuals, families and society. [electronic resource] by Fryns, J P Producer: 19901220 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	33.	X-linked mental retardation. [electronic resource] by Fryns, J P Producer: 19850814 In: Progress in clinical and biological research vol. 177 Availability: No items available. Save to lists Add to cart (remove)
	34.	Aarskog syndrome: the changing phenotype with age. [electronic resource] by Fryns, J P Producer: 19920716 In: American journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	The cardio-facio-cutaneous (CFC) syndrome and Robertsonian 15/22 translocation. [electronic resource] by Fryns, J P Producer: 19930121 In: Annales de genetique vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	36.	Klinefelter syndrome and the Xq11-22 region. [electronic resource] by Fryns, J P Producer: 19820225 In: Clinical genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Microcephaly/lymphedema and terminal deletion of the long arm of chromosome 13. [electronic resource] by Fryns, J P Producer: 19951019 In: American journal of medical genetics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	On the nosology of the Cornelia de Lange and Coffin-Siris syndromes. [electronic resource] by Fryns, J P Producer: 19860602 In: Clinical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	Screening for the fragile X syndrome: the necessity of international guidelines for molecular genetics predictive testing in general. [electronic resource] by Fryns, J P Producer: 19961017 In: Genetic counseling (Geneva, Switzerland) vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	40.	X-linked mental retardation with agenesis of the corpus callosum. [electronic resource] by Fryns, J P Producer: 19930506 In: American journal of medical genetics vol. 45 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 1120 results.