Omphalocele and gastroschisis: An 18-year review study von Hwang, Pei-Jen, Kousseff, Boris G.

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The Molecular Basis of X-Linked Spondyloepiphyseal Dysplasia Tarda von Gedeon, A.K., Tiller, G.E., Le Merrer, M., Heuertz, S., Tranebjaerg, L., Chitayat, D., Robertson, S., Glass, I.A., Savarirayan, R., Cole, W.G., Rimoin, D.L., Kousseff, B.G., Ohashi, H., Zabel, B., Munnich, A., Gecz, J., Mulley, J.C.

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Triploidy and trisomies in the offspring of a mother with a balanced translocation von Slavin, Thomas P., Kousseff, Boris G.

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'New' manifestations of BOR syndrome von Weber, Karen M, Kousseff, Boris G

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RET Mutation Screening in Familial Cutaneous Lichen Amyloidosis and in Skin Amyloidosis Associated With Multiple Endocrine Neoplasia von Hofstra, Robert M.W., Sijmons, Rolf H., Stelwagen, Tineke, Stulp, Rein P., Buys, Charles H.C.M., Kousseff, Boris G., Lips, Cornelis J.M., Steijlen, Peter M., Van Voorst Vader, Pieter C.

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Peripheral neuropathy in Ehlers-Danlos syndrome von Galan, Enrique, Kousseff, Boris G.

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NF1 mutation analysis using a combined heteroduplex/SSCP approach von Abernathy, Corinne R., Rasmussen, Sonja A., Stalker, Heather J., Zori, Roberto, Driscoll, Daniel J., Williams, Charles A., Kousseff, Boris G., Wallace, Margaret R.

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Expanded phenotype of cranioectodermal dysplasia (Sensenbrenner syndrome) von Amar, M. J. A., Sutphen, R., Kousseff, B. G.

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Collodion baby, sign of Tay syndrome von KOUSSEFF, B. G

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Sipple syndrome with lichen amyloidosis as a paracrinopathy: Pleiotropy, heterogeneity, or a contiguous gene? von Kousseff, Boris G., Espinoza, Carmen, Zamore, Gary A.

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The genetics of malignant melanomas von KOUSSEFF, B. G

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XXY male with X-linked dominant chondrodysplasia punctata (Happle syndrome) von Sutphen, Rebecca, Amar, Marcelo J., Kousseff, Boris G., Toomey, Kathleen E.

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Complex chromosome rearrangement with ankyloblepharon filiforme adnatum von Kousseff, B G, Papenhausen, P, Essig, Y P, Torres, M P

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Overgrowth Management in Klippel-Trenaunay-Weber and Proteus Syndromes von Guidera, Kenneth J, Brinker, Mark R, Kousseff, Boris G, Helal, Amira A, Pugh, Linda I, Ganey, Tim M, Ogden, John A

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Pleiotropy versus heterogeneity in Proteus syndrome von Kousseff, B G

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Sacral meningocele with conotruncal heart defects: a possible autosomal recessive trait von KOUSSEFF, B. G

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Endocrinopathies in Cornelia de Lange syndrome von Schwartz, I. David, Schwartz, Karen J., Kousseff, Boris G., Bercu, Barry B., Root, Allen W.

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Aniridia—Wilms tumor association von Kousseff, Boris G., Agatucci, Anthony

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Angioid Streaks Associated with Hereditary Spherocytosis von McLane, Nick J., Grizzard, W. Sanderson, Kousseff, Boris G., Hartmann, Robert C., Sever, Raymond J.

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Autosomal recessive type of whistling face syndrome in twins von Kousseff, B G, McConnachie, P, Hadro, T A

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