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	1.	Differentiated recurrence risk estimations in the Prader-Willi syndrome. [electronic resource] by Kennerknecht, I Producer: 19920807 In: Clinical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A genetic model for the Prader-Willi syndrome and its implication for Angelman syndrome. [electronic resource] by Kennerknecht, I Producer: 19921201 In: Human genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Prader-Willi syndrome and Sotos syndrome. [electronic resource] by Kennerknecht, I Producer: 19890601 In: Clinical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Intrauterine growth retardation associated with chromosomal aneuploidy confined to the placenta. Three observations: triple trisomy 6,21,22; trisomy 16; and trisomy 18. [electronic resource] by Kennerknecht, I Terinde, R Producer: 19910208 In: Prenatal diagnosis vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Reciprocal translocation t(1;15)(p36.2;p11.2): confirmation of a suggestive cytogenetic diagnosis by in situ hybridization and clinical case report on resulting monosomy (1p). [electronic resource] by Barbi, G Kennerknecht, I Klett, C Producer: 19920803 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.	Maternal transmission of ring chromosome 21. [electronic resource] by Kennerknecht, I Barbi, G Vogel, W Producer: 19910123 In: Human genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Dup(1q)(q42-->qter) syndrome: case report and review of literature. [electronic resource] by Kennerknecht, I Barbi, G Rodens, K Producer: 19940224 In: American journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A modified embryogenic model to explain embryonic/extraembryonic chromosomal inconsistencies. [electronic resource] by Kennerknecht, I Vogel, W Mehnert, K Producer: 19940609 In: Prenatal diagnosis vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	[Are there reproducible false-positive fra(X) findings in differential diagnosis of Martin-Bell syndrome?]. [electronic resource] by Kennerknecht, I Barbi, G Steinbach, P Producer: 19920107 In: Zeitschrift fur Kinder- und Jugendpsychiatrie vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	10.	Assignment of the human gene propionyl coenzyme A carboxylase, alpha-chain, (PCCA) to chromosome 13q32 by in situ hybridization. [electronic resource] by Kennerknecht, I Klett, C Hameister, H Producer: 19921201 In: Genomics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	A triploid fetus with a diploid placenta: proposal of a mechanism. [electronic resource] by Kennerknecht, I Just, W Vogel, W Producer: 19940209 In: Prenatal diagnosis vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Diagnosis of retinoblastoma in a presymptomatic stage after detection of interstitial chromosomal deletion 13q. [electronic resource] by Kennerknecht, I Barbi, G Greher, J Producer: 19941208 In: Ophthalmic genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Proliferation kinetics in native chorionic villus cells. [electronic resource] by Kennerknecht, I Baur-Aubele, S Vogel, W Producer: 19920220 In: Prenatal diagnosis vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	"Cutis tricolor": congenital hyper- and hypopigmented macules associated with a sporadic multisystem birth defect: an unusual example of twin spotting? [electronic resource] by Happle, R Barbi, G Eckert, D Kennerknecht, I Producer: 19971006 In: Journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Evaluation of amniotic fluid cell filtration: an experimental approach to early amniocentesis. [electronic resource] by Kennerknecht, I Krämer, S Grab, D Terinde, R Producer: 19930707 In: Prenatal diagnosis vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	How can the frequency of false-negative findings in prenatal diagnoses of fra(X) be reduced: experience with first trimester chorionic villi sampling. [electronic resource] by Kennerknecht, I Barbi, G Dahl, N Steinbach, P Producer: 19910521 In: American journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Introduction of early amniocentesis to routine prenatal diagnosis. [electronic resource] by Djalali, M Barbi, G Kennerknecht, I Terinde, R Producer: 19921223 In: Prenatal diagnosis vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Nuclear and chromosomal replication patterns in chorionic villi cells by bromodeoxyuridine labelling and DNA flow cytometry. [electronic resource] by Kennerknecht, I Baur-Aubele, S Terinde, R Vogel, W Producer: 19920904 In: Cell proliferation vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	The gene coding for the alpha-chain of human propionyl-CoA carboxylase maps to chromosome band 13q32. [electronic resource] by Kennerknecht, I Suormala, T Barbi, G Baumgartner, E R Producer: 19910212 In: Human genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	First trimester amniocentesis between the seventh and 13th weeks: evaluation of the earliest possible genetic diagnosis. [electronic resource] by Kennerknecht, I Baur-Aubele, S Grab, D Terinde, R Producer: 19920923 In: Prenatal diagnosis vol. 12 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 44 results.