Hypomagensemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpoint

This publication has 17 references indexed in Scilit:

• Report of the Fourth International Workshop on Human X Chromosome Mapping 1993 (Part 1 of 4)
  Cytogenetic and Genome Research, 1993
• Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region
  Human Genetics, 1991
• THE FRIEDREICH ATAXIA GENE IS ASSIGNED TO CHROMOSOME-9Q13-Q21 BY MAPPING OF TIGHTLY LINKED MARKERS AND SHOWS LINKAGE DISEQUILIBRIUM WITH D9S15
  1990
• Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome
  Human Genetics, 1986
• PRIMARY HYPOMAGNESAEMIA, AN AUTOSOMAL RECESSIVE INHERITED DISEASE?
  The Lancet, 1983
• PARATHYROID-HORMONE SECRETION AND RESPONSIVENESS TO PARATHYROID-HORMONE IN PRIMARY HYPOMAGNESEMIA
  1983
• X-Autosome translocations: Cytogenetic characteristics and their consequences
  Human Genetics, 1982
• [Primary hypomagnesemia. Clinical, diagnostic and therapeutic studies in three children (author's transl)].
  1979
• Tetany Due to Hypomagnesaemia with Secondary Hypocalcaemia
  Archives of Disease in Childhood, 1970
• Congenital Primary Hypomagnesemia, an Inborn Error of Metabolism?
  Acta Paediatrica, 1967