Publications in collaboration with researchers from Heidelberg University (10)

2016

  1. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

    Autophagy

  2. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

    Autophagy, Vol. 12, Núm. 1, pp. 1-222

2012

  1. Guidelines for the use and interpretation of assays for monitoring autophagy

    Autophagy, Vol. 8, Núm. 4, pp. 445-544

2000

  1. A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation

    American Journal of Human Genetics, Vol. 67, Núm. 3, pp. 563-573

1998

  1. Functional implications of the spectrum of mutations found in 234 cases with X-linked juvenile retinoschisis (XLRS)

    Human Molecular Genetics, Vol. 7, Núm. 7, pp. 1185-1192

1997

  1. Comparative mapping of Xp22 genes in hominoids - evolutionary linear instability of their Y homologues

    Chromosome Research, Vol. 5, Núm. 3, pp. 167-176

1996

  1. Mental Retardation in a Boy with an Interstitial Deletion at Xp22.3 Involving STS, KALI, and OA1: Implication for the MRX Locus

    American Journal of Medical Genetics - Seminars in Medical Genetics, Vol. 64, Núm. 4, pp. 583-587

1995

  1. A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy

    Cell, Vol. 81, Núm. 1, pp. 15-25

  2. High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)

    Genomics, Vol. 26, Núm. 2, pp. 229-238

1992

  1. Physical mapping of 14 new DNA markers isolated from the human distal Xp region

    Genomics, Vol. 13, Núm. 1, pp. 167-175