Second‐trimester molecular prenatal diagnosis of sporadic Apert syndrome following suspicious ultrasound findings
Ferreira, J. C., Carter, S. M., Bernstein, P. S., Jabs, E. W., Glickstein, J. S., Marion, R. W., Baergen, R. N., Gross, S. J.
Published in Ultrasound in obstetrics & gynecology (01.12.1999)
Published in Ultrasound in obstetrics & gynecology (01.12.1999)
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Journal Article
Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22
Quaderi, N A, Schweiger, S, Gaudenz, K, Franco, B, Rugarli, E I, Berger, W, Feldman, G J, Volta, M, Andolfi, G, Gilgenkrantz, S, Marion, R W, Hennekam, R C, Opitz, J M, Muenke, M, Ropers, H H, Ballabio, A
Published in Nature genetics (01.11.1997)
Published in Nature genetics (01.11.1997)
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Journal Article
Marshall Syndrome and a Defect at the COL11A1 Locus
Shanske, Alan, Bogdanow, Anna, Shprintzen, Robert J., Marion, Robert W.
Published in American journal of human genetics (01.11.1998)
Published in American journal of human genetics (01.11.1998)
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Journal Article
Spondyloepiphyseal dysplasia congenita : genetic linkage to type II collagen (COL2AI)
ANDERSON, I. J, GOLDBERG, R. B, MARION, R. W, UPHOLT, W. B, TSIPOURAS, P
Published in American journal of human genetics (01.05.1990)
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Published in American journal of human genetics (01.05.1990)
Journal Article
Prenatal diagnosis of type 2 Pfeiffer syndrome
Bernstein, P S, Gross, S J, Cohen, D J, Tiller, G R, Shanske, A L, Bombard, A T, Marion, R W
Published in Ultrasound in obstetrics & gynecology (01.12.1996)
Published in Ultrasound in obstetrics & gynecology (01.12.1996)
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Journal Article
Vascular plant community dynamics following hexazinone site preparation in the lower Coastal Plain
Wilkins R.N, Marion W.R, Neary D.G, Tanner G.W
Published in Canadian journal of forest research (01.10.1993)
Published in Canadian journal of forest research (01.10.1993)
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Journal Article
Hemimaxillofacial dysplasia: A report of two new cases and further delineation of the disorder
Paticoff, Kenneth, Marion, Robert W, Shprintzen, Robert J, Shanske, Alan L, Eisig, Sidney B
Published in Oral surgery, oral medicine, oral pathology, oral radiology and endodontics (01.04.1997)
Published in Oral surgery, oral medicine, oral pathology, oral radiology and endodontics (01.04.1997)
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Journal Article
Elevation of serum beta-hexosaminidase and alpha-D-mannosidase in type 2 Gaucher disease: a clinical and biochemical study
Chitayat, D, Nakagawa, S, Marion, R W, Sachs, G S, Shinnar, S, Llena, J F, Nitowsky, H M
Published in Journal of inherited metabolic disease (01.06.1987)
Published in Journal of inherited metabolic disease (01.06.1987)
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Journal Article
DNA testing for neurofibromatosis type 1
Karasik, Jeffrey B., Marion, Robert W., Javed, Ali A.
Published in The Journal of pediatrics (01.11.1992)
Published in The Journal of pediatrics (01.11.1992)
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Journal Article
Trisomy 18 score: A rapid, reliable diagnostic test for trisomy 18
Marion, Robert W., Chitayat, David, Hutcheon, R. Gordon, Neidich, Julie A., Zackal, Elaine H., Singer, Lewis P., Warman, Matthew
Published in The Journal of pediatrics (01.07.1988)
Published in The Journal of pediatrics (01.07.1988)
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Journal Article
Late-onset psychosis in the velo-cardio-facial syndrome
Shprintzen, R J, Goldberg, R, Golding-Kushner, K J, Marion, R W
Published in American journal of medical genetics (01.01.1992)
Published in American journal of medical genetics (01.01.1992)
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Journal Article
Further delineation of the Opitz G/BBB syndrome: report of an infant with complex congenital heart disease and bladder exstrophy, and review of the literature
Jacobson, Z, Glickstein, J, Hensle, T, Marion, R W
Published in American journal of medical genetics (07.07.1998)
Published in American journal of medical genetics (07.07.1998)
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Journal Article
Apparent dominant transmission of the Rubinstein-Taybi syndrome
Marion, R W, Garcia, D M, Karasik, J B
Published in American journal of medical genetics (15.05.1993)
Published in American journal of medical genetics (15.05.1993)
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