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

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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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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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Diabetic embryopathy von Kousseff, B G

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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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Analysis of CpG C-to-T mutations in neurofibromatosis type 1 von Krkljus, Sofia, Abernathy, Corinne R., Johnson, Jennifer S., Williams, Charles A., Driscoll, Daniel J., Zori, Roberto, Stalker, Heather J., Rasmussen, Sonja A., Collins, Francis S., Kousseff, Boris G., Baumbach, Lisa, Wallace, Margaret R.

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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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Prenatal Diagnosis of Hypophosphatasia von KOUSSEFF, BORIS G, MULIVOR, RICHARD A

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Uniparental isodisomy of chromosome 14 in two cases: An abnormal child and a normal adult von Papenhausen, Peter R., Mueller, O. Thomas, Johnson, Virginia P., Sutcliffe, Maxine, Diamond, Theresa M., Kousseff, Boris G.

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

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Three cell line mosaicism involving structural and numerical abnormalities of chromosome 18 in a 3.5-Year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XX von Sutcliffe, Maxine J., Mueller, O. Thomas, Kousseff, Boris G., Dumont, Doris P., McFarland, Julia A., Mawani, Fayaz, Conforto, Danielle, Ranells, Judith D.

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ROENTGENOGRAPHIC FINDINGS IN FUCOSIDOSIS TYPE 2 von BRILL, PAULA W, BERATIS, NICHOLAS G, KOUSSEFF, BORIS G, HIRSCHHORN, KURT

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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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Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome von Tantravahi, Umadevi, Nicholls, Robert D., Stroh, Helene, Ringer, Steven, Neve, Rachael L., Kaplan, Lawrence, Wharton, Robert, Wurster-Hill, Doris, Graham Jr, John M., Cantú, Eduardo S., Frias, Jaime L., Kousseff, Boris G., Latt, Samuel A.

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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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Two NF1 mutations: Frameshift in the GAP-related domain, and loss of two codons toward the 3′ end of the gene von Abernathy, Corinne R., Colman, Steven D., Kousseff, Boris G., Wallace, Margaret R.

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Gestational diabetes mellitus (class A): A human teratogen? von Kousseff, Boris G.

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