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	81.	Interstitial deletion of chromosome 11 (q22.3-q23.2) in a boy with mild developmental delay. [electronic resource] by Syrrou, M Fryns, J P Producer: 20020110 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	82.	Re: First-trimester features of Fowler syndrome (hydrocephaly-hydranencephaly proliferative vasculopathy). [electronic resource] by Witters, I Fryns, J-P Producer: 20030804 In: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	83.	Acro-osteolysis and symphalangism mutations. [electronic resource] by Debeer, P Fryns, J-P Producer: 20050525 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	84.	Human chromosome fragility. [electronic resource] by Lukusa, T Fryns, J P Producer: 20080619 In: Biochimica et biophysica acta vol. 1779 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	85.	Prenatal diagnosis of trisomy 21: registration results from a single genetic center. [electronic resource] by Witters, I Fryns, J P Producer: 20080909 In: Genetic counseling (Geneva, Switzerland) vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	86.	Interstital deletion of 13q associated with retinoblastoma and congenital malformations. [electronic resource] by Petit, P Fryns, J P Producer: 19791220 In: Annales de genetique vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	87.	[Tetrasomy 12p (Pallister-Killian syndrome): possible diagnosis before the age of a year]. [electronic resource] by Chrzanowska, K Fryns, J P Producer: 19900410 In: Journal de genetique humaine vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	88.	Ring chromosome 21 in the mother and 21/21 translocation in the fetus: karyotype: 45,XX,-21,-21,+t(21;21)(p11;q11). [electronic resource] by Fryns, J P Kleczkowska, A Producer: 19871214 In: Annales de genetique vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	89.	Reciprocal translocation mosaicism in man. [electronic resource] by Fryns, J P Kleczkowska, A Producer: 19870127 In: American journal of medical genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	90.	Distal osteolysis, short stature, mental retardation, and characteristic facial appearance: delineation of an autosomal recessive subtype of essential osteolysis. [electronic resource] by Petit, P Fryns, J P Producer: 19861231 In: American journal of medical genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	91.	Extreme growth failure and kyphoscoliosis as complications of the distal trisomy 10q syndrome. [electronic resource] by Soekarman, D Fryns, J P Producer: 19920910 In: Genetic counseling (Geneva, Switzerland) vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	92.	The Fryns syndrome: diaphragmatic defects, craniofacial dysmorphism, and distal digital hypoplasia. Further evidence for autosomal recessive inheritance. [electronic resource] by Meinecke, P Fryns, J P Producer: 19860219 In: Clinical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	93.	A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasia. [electronic resource] by Fryns, J P Moerman, P Producer: 19950802 In: Genetic counseling (Geneva, Switzerland) vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	94.	New MR/MCA syndrome with distinct facial appearance and general habitus, broad and webbed neck, hypoplastic inverted nipples, epilepsy, and pachygyria of the frontal lobes. [electronic resource] by Fryns, J P Aftimos, S Producer: 20000802 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	95.	Early development (5 to 48 months) in Williams syndrome. A study of 14 children. [electronic resource] by Plissart, L Fryns, J P Producer: 19991227 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	96.	Interstitial deletion 2p accompanied by marker chromosome formation of the deleted segment resulting in a stable acentric marker chromosome. [electronic resource] by Petit, P Fryns, J P Producer: 19980326 In: Genetic counseling (Geneva, Switzerland) vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	97.	Oral-facial-digital syndrome type IV (Mohr-Majewski syndrome): a fetopathological study. [electronic resource] by Moerman, P Fryns, J P Producer: 19980710 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	98.	A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasia: evidence for autosomal recessive inheritance. [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)
	99.	Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her child. [electronic resource] by Moerman, P Fryns, J P Producer: 19961209 In: American journal of medical genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	100.	Multiple-marker screen positive results in Rubinstein-Taybi syndrome. [electronic resource] by Fryns, J P Ramaekers, P Producer: 19970227 In: Prenatal diagnosis vol. 16 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.