Wirth B - Search Results

1

Extended phenotype of pontocerebellar hypoplasia with infantile spinal muscular atrophy.

Rudnik-Schöneborn S, Sztriha L, Aithala GR, Houge G, Laegreid LM, Seeger J, Huppke M, Wirth B, Zerres K. Rudnik-Schöneborn S, et al. Among authors: wirth b. Am J Med Genet A. 2003 Feb 15;117A(1):10-7. doi: 10.1002/ajmg.a.10863. Am J Med Genet A. 2003. PMID: 12548734

2

Childhood manifestation of autosomal dominant polycystic kidney disease: no evidence for genetic heterogeneity.

Gal A, Wirth B, Kääriäinen H, Lucotte G, Landais P, Gillessen-Kaesbach G, Müller-Wiefel DE, Zerres K. Gal A, et al. Among authors: wirth b. Clin Genet. 1989 Jan;35(1):13-9. doi: 10.1111/j.1399-0004.1989.tb02900.x. Clin Genet. 1989. PMID: 2924430

3

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. Hum Genet. 1987 Nov;77(3):221-2. doi: 10.1007/BF00284473. Hum Genet. 1987. PMID: 3479385

4

Genetic basis of adult-onset spinal muscular atrophy.

Zerres K, Rudnik-Schöneborn S, Forkert R, Wirth B. Zerres K, et al. Among authors: wirth b. Lancet. 1995 Oct 28;346(8983):1162. doi: 10.1016/s0140-6736(95)91835-3. Lancet. 1995. PMID: 7475624 No abstract available.

5

Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: association of marker genotype with disease severity and candidate cDNAs.

Wirth B, Hahnen E, Morgan K, DiDonato CJ, Dadze A, Rudnik-Schöneborn S, Simard LR, Zerres K, Burghes AH. Wirth B, et al. Hum Mol Genet. 1995 Aug;4(8):1273-84. doi: 10.1093/hmg/4.8.1273. Hum Mol Genet. 1995. PMID: 7581364

6

Prenatal prediction in families with autosomal recessive proximal spinal muscular atrophy (5q11.2-q13.3): molecular genetics and clinical experience in 109 cases.

Wirth B, Rudnik-Schöneborn S, Hahnen E, Röhrig D, Zerres K. Wirth B, et al. Prenat Diagn. 1995 May;15(5):407-17. doi: 10.1002/pd.1970150503. Prenat Diagn. 1995. PMID: 7644431

7

Exclusion of the gene locus for spinal muscular atrophy on chromosome 5q in a family with infantile olivopontocerebellar atrophy (OPCA) and anterior horn cell degeneration.

Rudnik-Schöneborn S, Wirth B, Röhrig D, Saule H, Zerres K. Rudnik-Schöneborn S, et al. Among authors: wirth b. Neuromuscul Disord. 1995 Jan;5(1):19-23. doi: 10.1016/0960-8966(94)e0025-4. Neuromuscul Disord. 1995. PMID: 7719136

8

Mapping of the spinal muscular atrophy (SMA) gene to a 750-kb interval flanked by two new microsatellites.

Wirth B, el-Agwany A, Baasner A, Burghes A, Koch A, Dadze A, Piechaczeck-Wappenschmidt B, Rudnik-Schöneborn S, Zerres K, Schönling J. Wirth B, et al. Eur J Hum Genet. 1995;3(1):56-60. doi: 10.1159/000472274. Eur J Hum Genet. 1995. PMID: 7767657

9

Large linkage analysis in 100 families with autosomal recessive spinal muscular atrophy (SMA) and 11 CEPH families using 15 polymorphic loci in the region 5q11.2-q13.3.

Wirth B, Pick E, Leutner A, Dadze A, Voosen B, Knapp M, Piechaczek-Wappenschmidt B, Rudnik-Schöneborn S, Schönling J, Cox S, et al. Wirth B, et al. Genomics. 1994 Mar 1;20(1):84-93. doi: 10.1006/geno.1994.1130. Genomics. 1994. PMID: 7912691

10

Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophy.

DiDonato CJ, Morgan K, Carpten JD, Fuerst P, Ingraham SE, Prescott G, McPherson JD, Wirth B, Zerres K, Hurko O, et al. DiDonato CJ, et al. Among authors: wirth b. Am J Hum Genet. 1994 Dec;55(6):1218-29. Am J Hum Genet. 1994. PMID: 7977383 Free PMC article.

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