Scherer G - Search Results

1

SOX20, a new member of the SOX gene family, is located on chromosome 17p13.

Meyer J, Wirth J, Held M, Schempp W, Scherer G. Meyer J, et al. Among authors: scherer g. Cytogenet Cell Genet. 1996;72(2-3):246-9. doi: 10.1159/000134200. Cytogenet Cell Genet. 1996. PMID: 8978787

2

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9.

Wagner T, Wirth J, Meyer J, Zabel B, Held M, Zimmer J, Pasantes J, Bricarelli FD, Keutel J, Hustert E, Wolf U, Tommerup N, Schempp W, Scherer G. Wagner T, et al. Among authors: scherer g. Cell. 1994 Dec 16;79(6):1111-20. doi: 10.1016/0092-8674(94)90041-8. Cell. 1994. PMID: 8001137

3

Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9.

Wirth J, Wagner T, Meyer J, Pfeiffer RA, Tietze HU, Schempp W, Scherer G. Wirth J, et al. Among authors: scherer g. Hum Genet. 1996 Feb;97(2):186-93. doi: 10.1007/BF02265263. Hum Genet. 1996. PMID: 8566951

4

A somatic cell hybrid panel for distal 17q: GDIA1 maps to 17q25.3.

Wagner T, Tommerup N, Wirth J, Leffers H, Zimmer J, Back E, Weissenbach J, Scherer G. Wagner T, et al. Among authors: scherer g. Cytogenet Cell Genet. 1997;76(3-4):172-5. doi: 10.1159/000134538. Cytogenet Cell Genet. 1997. PMID: 9186513

5

Three novel SRY mutations in XY gonadal dysgenesis and the enigma of XY gonadal dysgenesis cases without SRY mutations.

Scherer G, Held M, Erdel M, Meschede D, Horst J, Lesniewicz R, Midro AT. Scherer G, et al. Cytogenet Cell Genet. 1998;80(1-4):188-92. doi: 10.1159/000014978. Cytogenet Cell Genet. 1998. PMID: 9678356

6

An SRY-negative 47,XXY mother and daughter.

Röttger S, Schiebel K, Senger G, Ebner S, Schempp W, Scherer G. Röttger S, et al. Among authors: scherer g. Cytogenet Cell Genet. 2000;91(1-4):204-7. doi: 10.1159/000056845. Cytogenet Cell Genet. 2000. PMID: 11173857

7

Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlations.

Meyer J, Südbeck P, Held M, Wagner T, Schmitz ML, Bricarelli FD, Eggermont E, Friedrich U, Haas OA, Kobelt A, Leroy JG, Van Maldergem L, Michel E, Mitulla B, Pfeiffer RA, Schinzel A, Schmidt H, Scherer G. Meyer J, et al. Among authors: scherer g. Hum Mol Genet. 1997 Jan;6(1):91-8. doi: 10.1093/hmg/6.1.91. Hum Mol Genet. 1997. PMID: 9002675 Free article.

8

Localization of Y chromosome sequences and X chromosomal replication studies in XX males.

Schempp W, Müller G, Scherer G, Bohlander SK, Rommerskirch W, Fraccaro M, Wolf U. Schempp W, et al. Among authors: scherer g. Hum Genet. 1989 Jan;81(2):144-8. doi: 10.1007/BF00293890. Hum Genet. 1989. PMID: 2912884

9

Duplication of an Xp segment that includes the ZFX locus causes sex inversion in man.

Scherer G, Schempp W, Baccichetti C, Lenzini E, Bricarelli FD, Carbone LD, Wolf U. Scherer G, et al. Hum Genet. 1989 Feb;81(3):291-4. doi: 10.1007/BF00279008. Hum Genet. 1989. PMID: 2921042

10

Molecular biology of the human Y chromosome.

Wolf U, Schempp W, Scherer G. Wolf U, et al. Among authors: scherer g. Rev Physiol Biochem Pharmacol. 1992;121:147-213. doi: 10.1007/BFb0033195. Rev Physiol Biochem Pharmacol. 1992. PMID: 1485072 Review. No abstract available.

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