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Items: 7

1.
2.

Paracentric inversions in man.

Madan K, Seabright M, Lindenbaum RH, Bobrow M.

J Med Genet. 1984 Dec;21(6):407-12. Review.

3.

The inheritance of a structural anomaly of one chromosome No. 16 in a kindred (46,16-,C+).

Chemke J, Robinson A.

J Med Genet. 1971 Sep;8(3):346-50. No abstract available.

4.
5.

C-band length variability and reproductive wastage.

Rodriguez-Gómez MT, Martín-Sempere MJ, Abrisqueta JA.

Hum Genet. 1987 Jan;75(1):56-61.

PMID:
3804333
6.

Molecular characterization of the smallest secondary constriction region (qh) of human chromosome 16.

Verma RS, Luke S, Mathews T, Conte RA.

Genet Anal Tech Appl. 1992 Oct-Dec;9(5-6):140-2.

PMID:
1363590
7.

'De novo' trisomy 16q11 to pter.

Dallapiccola B, Curatolo P, Balestrazzi P.

Hum Genet. 1979 May 23;49(1):1-6.

PMID:
468236

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