Neugebauer M - Search Results

1

Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp.

Gal A, Schinzel A, Orth U, Fraser NA, Mollica F, Craig IW, Kruse T, Mächler M, Neugebauer M, Bleeker-Wagemakers LM. Gal A, et al. Among authors: neugebauer m. Hum Genet. 1989 Mar;81(4):315-8. doi: 10.1007/BF00283682. Hum Genet. 1989. PMID: 2564836

2

Gene localization in a family with X-linked syndromal mental retardation (Prieto syndrome).

Watty A, Prieto F, Beneyto M, Neugebauer M, Gal A. Watty A, et al. Among authors: neugebauer m. Am J Med Genet. 1991 Feb-Mar;38(2-3):234-9. doi: 10.1002/ajmg.1320380213. Am J Med Genet. 1991. PMID: 1673297

3

Gene for non-specific X-linked mental retardation maps in the pericentromeric region.

Samanns C, Albrecht R, Neugebauer M, Neri G, Gal A. Samanns C, et al. Among authors: neugebauer m. Am J Med Genet. 1991 Feb-Mar;38(2-3):224-7. doi: 10.1002/ajmg.1320380210. Am J Med Genet. 1991. PMID: 2018062

4

Linkage analysis in X-linked ichthyosis (steroid sulfatase deficiency).

Wirth B, Herrmann FH, Neugebauer M, Gillard EF, Wulff K, Stein C, von Figura K, Ferguson-Smith MA, Gal A. Wirth B, et al. Among authors: neugebauer m. Hum Genet. 1988 Oct;80(2):191-2. doi: 10.1007/BF00702868. Hum Genet. 1988. PMID: 3169744

5

Posthumous diagnosis of X-linked retinoschisis using DNA analysis.

van Schooneveld MJ, Bleeker-Wagemakers EM, Orth U, Neugebauer M, Hogenkamp T, Gal A. van Schooneveld MJ, et al. Among authors: neugebauer m. Ophthalmic Paediatr Genet. 1990 Dec;11(4):293-7. doi: 10.3109/13816819009015716. Ophthalmic Paediatr Genet. 1990. PMID: 1982897

6

Two different genes for X-linked retinitis pigmentosa.

Wirth B, Denton MJ, Chen JD, Neugebauer M, Halliday FB, van Schooneveld M, Donald J, Bleeker-Wagemakers EM, Pearson PL, Gal A. Wirth B, et al. Among authors: neugebauer m. Genomics. 1988 Apr;2(3):263-6. doi: 10.1016/0888-7543(88)90011-0. Genomics. 1988. PMID: 3397063

7

[Norrie syndrome: identification of carriers by segregation analysis with flanking DNA markers].

Körner J, Uhlhaas S, Neugebauer M, Gal A. Körner J, et al. Among authors: neugebauer m. Fortschr Ophthalmol. 1989;86(1):78-81. Fortschr Ophthalmol. 1989. PMID: 2566566 German.

8

Cystic fibrosis: typing 89 German families with linked DNA probes.

Weber J, Aulehla-Scholz C, Kaiser R, Eigel A, Neugebauer M, Horst J, Olek K. Weber J, et al. Among authors: neugebauer m. Hum Genet. 1988 Dec;81(1):54-6. doi: 10.1007/BF00283729. Hum Genet. 1988. PMID: 2904405

9

Autosomal recessive and dominant forms of polycystic kidney disease are not allelic.

Wirth B, Zerres K, Fischbach M, Claus D, Neumann HP, Lennert T, Brodehl J, Neugebauer M, Müller-Wiefel DE, Geisert J, et al. Wirth B, et al. Among authors: neugebauer m. Hum Genet. 1987 Nov;77(3):221-2. doi: 10.1007/BF00284473. Hum Genet. 1987. PMID: 3479385

10

MASA syndrome: clinical variability and linkage analysis.

Rietschel M, Friedl W, Uhlhaas S, Neugebauer M, Heimann D, Zerres K. Rietschel M, et al. Among authors: neugebauer m. Am J Med Genet. 1991 Oct 1;41(1):10-4. doi: 10.1002/ajmg.1320410104. Am J Med Genet. 1991. PMID: 1951449

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