Terminal deletion of the long arm of chromosome 1 in a malformed newborn

Author:

Kessel E.,Pfeiffer R. A.,Blanke W.,Schwarz J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference8 articles.

1. Bobrow, M., Emerson, P. M., Spriggs, A. I., Ellis, H. L.: Ring-1-chromosome, microcephalic dwarfism, and acute myeloid leukemia. Am. J. Dis. Child. 126, 257?260 (1973)

2. Gordon, R. R., Cooke, P.: Ring-1-chromosome and microcephalic dwarfism. Lancet 1964II, 1212?1213

3. Koivisto, M., Akerblom, H. K., Remes, M., Chapelle, A. de la: Primary hypothyroidism, growth hormone deficiency and congenital malformations in a child with the karyotype 46,XY,del (1)(q25q32). Acta paediatr. Scand. 65, 513?518 (1976)

4. Mankinen, C. B., Sears, J. W., Alvarez, V. R.: Terminal (1)(q43) long arm deletion of chromosome no. 1 in a three-year-old female. Birth Defects: Orig. Art. Ser. XII 5, 131?136 (1976)

5. Monier, R.: 5 S RNA. In: Ribosomes, M. Nomura, A. Tissi�res, and P. Lengyel, eds., pp. 141?168. Cold Spring Harbor Laboratory 1974

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