HOMOZYGOUS FORM OF PELGER-HUETS NUCLEAR ANOMALY IN MAN

[1] BEGEMANN NH, 1951, MAANDSCHR KINDERGENE, V19, P338

[2] DONZELOT E, 1946, PRESSE MED, V54, P333

[3] HUET GJ, 1931, NED TIJDSCHR GENEES, V4, P5956

[4] HUET GJ, 1931, NED TIJDSCHR GENEES, V3, P4959

[5] HUET GJ, 1932, KLIN WOCHENSCHR, V11, P1264

[6] LEITNER SJ, 1949, BONE MARROW BIOPSY

[7] LEITNER SJ, 1938, NED TIJDSCHR GENEES, V82, P3953

[8] THE PELGER-ANOMALY IN MAN AND RABBIT - A MENDELIAN CHARACTER OF THE NUCLEI OF THE LEUCOCYTES [J]. JOURNAL OF HEREDITY, 1950, 41 (05) : 131 - 137

[9] NACHTSHEIM H., 1942, Erbarzt, V10, P175

[10] NACHTSHEIM H, 1950, ARCH KLAUSSTIFT VERE, V25, P566

[1] BEGEMANN NH, 1951, MAANDSCHR KINDERGENE, V19, P338

[2] DONZELOT E, 1946, PRESSE MED, V54, P333

[3] HUET GJ, 1931, NED TIJDSCHR GENEES, V4, P5956

[4] HUET GJ, 1931, NED TIJDSCHR GENEES, V3, P4959

[5] HUET GJ, 1932, KLIN WOCHENSCHR, V11, P1264

[6] LEITNER SJ, 1949, BONE MARROW BIOPSY

[7] LEITNER SJ, 1938, NED TIJDSCHR GENEES, V82, P3953

[8] THE PELGER-ANOMALY IN MAN AND RABBIT - A MENDELIAN CHARACTER OF THE NUCLEI OF THE LEUCOCYTES [J]. JOURNAL OF HEREDITY, 1950, 41 (05) : 131 - 137

[9] NACHTSHEIM H., 1942, Erbarzt, V10, P175

[10] NACHTSHEIM H, 1950, ARCH KLAUSSTIFT VERE, V25, P566