Interstitial deletion of the long arm of chromosome 2: A case report and review of the literature

[1]  B. Martin-Pont,et al.  De novo interstitial deletion of the long arm of chromosome 7:46,XY,del(7)(q23;q32). , 1985, Annales de genetique.

[2]  J. M. Sánchez,et al.  A case of deletion 2q35----qter and a peculiar phenotype. , 1984, Journal of medical genetics.

[3]  X. Carbonell,et al.  DE NOVO INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 2 IN A MALFORMED NEWBORN WITH A KARYOTYPE: 46, XY, del(2)(q12q14) , 1983, Acta paediatrica Scandinavica.

[4]  K. Hansen,et al.  Deletion 2q: two new cases with karyotypes 46,XY,del(2)(q31q33) and 46,XX,del(2)(q36). , 1983, Journal of medical genetics.

[5]  J. Opitz,et al.  Interstitial deletion 2q31→q33 , 1983 .

[6]  J. Rogers,et al.  Identical multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to del(2)(q32) in two sisters with intrachromosomal insertional translocation in their father. , 1983, American journal of medical genetics.

[7]  F. Shabtai,et al.  Partial monosomy of chromosome 2. Delineable syndrome of deletion 2 (q23-q31). , 1982, Annales de genetique.

[8]  K. Taysi,et al.  Interstitial deletion of the long arm of chromosome 2: case report and review of literature. , 1981, Annales de genetique.

[9]  T. McConnell,et al.  Partial deletion of chromosome 2 mimicking a phenotype of trisomy 18: case report with autopsy. , 1980, Human pathology.

[10]  T. Ikeuchi,et al.  Accumulation of Early Mitotic Cells in Ethidium Bromide-Treated Human Lymphocyte Cultures , 1979 .

[11]  H. Harris,et al.  Handbook of enzyme electrophoresis in human genetics , 1976 .

[12]  H. Harris,et al.  GENETICAL STUDIES ON HUMAN RED CELL ACID PHOSPHATASE. , 1964, American journal of human genetics.

[13]  H. Bergmeyer.  Methods of Enzymatic Analysis , 2019 .