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	1.	A remarkable pharynx fibroma. [electronic resource] by SMITS, A P Producer: 19981101 In: Practica oto-rhino-laryngologica vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Menstrual disorders and endocrine profiles in fragile X carriers prior to 40 years of age: a pilot study. [electronic resource] by Braat, D D Smits, A P Thomas, C M Producer: 19990610 In: American journal of medical genetics vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Recombination of DXS548 (RS46) with the FRAXA locus. [electronic resource] by Dreesen, J C Smits, A P van Oost, B A Producer: 19941116 In: American journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A case of AMMoL with 8/21 translocation and loss of the Y as probably secondary events. [electronic resource] by Hustinx, T W Burghouts, J T Scheres, J M Smits, A P Producer: 19800327 In: Cancer vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Penetrance estimate of the fra(X) gene using Pointer versus direct estimate. [electronic resource] by de Haan, A F Smits, A P Smeets, D F van Oost, B A 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)
	6.	[Perinatal asphyxia as incorrect explanation for mental retardation]. [electronic resource] by Tuerlings, J H A M Smits, A P T van den Berg, P P Producer: 20021217 In: Nederlands tijdschrift voor geneeskunde vol. 146 Availability: No items available. Save to lists Add to cart (remove)
	7.	Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptives. [electronic resource] by Hundscheid, R D Braat, D D Kiemeney, L A Smits, A P Thomas, C M Producer: 20010503 In: Human reproduction (Oxford, England) vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patients. [electronic resource] by de Graaff, E Rouillard, P Willems, P J Smits, A P Rousseau, F Oostra, B A Producer: 19950516 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Monosomy 7 in two patients with a myeloproliferative disorder. [electronic resource] by Boetius, G Hustinx, T W Smits, A P Scheres, J M Rutten, F J Haanen, C Producer: 19780218 In: British journal of haematology vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Longitudinal changes in cognitive-behavioral levels in three children with FRAXE. [electronic resource] by Fisch, G S Carpenter, N J Simensen, R Smits, A P van Roosmalen, T Hamel, B C Producer: 19990624 In: American journal of medical genetics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Validation of linkage-based DNA-diagnosis of fragile X gene carriers with the CGG repeat probe. [electronic resource] by van Oost, B A Smits, A P Dreesen, J C van den Ouweland, A M Oostra, B A 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)
	12.	Experts' opinions on the benefit of an incidental prenatal diagnosis of sex chromosomal aneuploidy: a qualitative interview survey. [electronic resource] by Pieters, J J P M Verhaak, C M Braat, D D M van Leeuwen, E Smits, A P T Producer: 20130430 In: Prenatal diagnosis vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Psychometric assessment of families with X-linked mental retardation. [electronic resource] by van Roosmalen, T Smits, A P Thoonen, G H Hamel, B C Assman-Hulmans, C F Gabreels, F J Producer: 19990610 In: American journal of medical genetics vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findings. [electronic resource] by Hamel, B C Smits, A P Otten, B J van den Helm, B Ropers, H H Mariman, E C Producer: 19961120 In: American journal of medical genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Familial idiopathic premature ovarian failure: an overrated and underestimated genetic disease? [electronic resource] by van Kasteren, Y M Hundscheid, R D Smits, A P Cremers, F P van Zonneveld, P Braat, D D Producer: 19991124 In: Human reproduction (Oxford, England) vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Penetrance of fra(X) gene: influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting male. [electronic resource] by Smits, A P van Oost, B A de Haan, A F Hamel, B C Dreesen, J C Smeets, D F 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)
	17.	Female carriers of fragile X premutations have no increased risk for additional diseases other than premature ovarian failure. [electronic resource] by Hundscheid, R D L Smits, A P T Thomas, C M G Kiemeney, L A L M Braat, D D M Producer: 20030520 In: American journal of medical genetics. Part A vol. 117A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Incidental prenatal diagnosis of sex chromosome aneuploidies: health, behavior, and fertility. [electronic resource] by Pieters, J J P M Kooper, A J A van Kessel, A Geurts Braat, D D M Smits, A P T Producer: 20120823 In: ISRN obstetrics and gynecology vol. 2011 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report. [electronic resource] by Mundhofir, F E P Kooper, A J A Winarni, T I Smits, A P T Faradz, S M H Hamel, B C J Producer: 20100514 In: Genetic counseling (Geneva, Switzerland) vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	20.	DXS539, a polymorphic DNA marker proximal of the fragile-X gene. [electronic resource] by Dreesen, J C van den Hurk, J A Smits, A P van den Ouweland, A M Markslag, P W van Oost, B A Producer: 19930419 In: Human genetics vol. 91 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 39 results.