Lin CC - Search Results

1

Recurrent de novo interstitial deletion of 16q in two mentally retarded sisters.

Hoo JJ, Lowry RB, Lin CC, Haslam RH. Hoo JJ, et al. Among authors: lin cc. Clin Genet. 1985 Apr;27(4):420-5. doi: 10.1111/j.1399-0004.1985.tb02287.x. Clin Genet. 1985. PMID: 3995793

2

Interstitial deletion for a region in the long arm of chromosome 16.

Lin CC, Lowry RB, Snyder FF. Lin CC, et al. Hum Genet. 1983;65(2):134-8. doi: 10.1007/BF00286649. Hum Genet. 1983. PMID: 6654327

3

Multiple, variable-sized, minute marker chromosomes.

Hoo JJ, Lin CC. Hoo JJ, et al. Among authors: lin cc. Am J Med Genet. 1988 Feb;29(2):361-3. doi: 10.1002/ajmg.1320290215. Am J Med Genet. 1988. PMID: 3354607 No abstract available.

4

Familial paracentric inversions inv(2)(q31q35) and inv(8)(q22.3q24.13) ascertained through reproductive abnormalities.

Lin CC, Bowen P, Hoo JJ. Lin CC, et al. Hum Genet. 1987 Jan;75(1):84-7. doi: 10.1007/BF00273848. Hum Genet. 1987. PMID: 3804335

5

A de novo case of trisomy 10p: gene dosage studies of hexokinase, inorganic pyrophosphatase and adenosine kinase.

Snyder FF, Lin CC, Rudd NL, Shearer JE, Heikkila EM, Hoo JJ. Snyder FF, et al. Among authors: lin cc. Hum Genet. 1984;67(2):187-9. doi: 10.1007/BF00272998. Hum Genet. 1984. PMID: 6146563

6

Two cases of variant Philadelphia chromosome resulting from translocation (21;22) and (3;19;22).

Heikkila E, Lin CC, Hoo JJ. Heikkila E, et al. Among authors: lin cc. Cancer Genet Cytogenet. 1984 Feb;11(2):223-6. doi: 10.1016/0165-4608(84)90117-1. Cancer Genet Cytogenet. 1984. PMID: 6581860

7

Selective IgA deficiency with 18q+ and 18q-- karyotypic anomalies.

Lewkonia RM, Lin CC, Haslam RH. Lewkonia RM, et al. Among authors: lin cc. J Med Genet. 1980 Dec;17(6):453-6. doi: 10.1136/jmg.17.6.453. J Med Genet. 1980. PMID: 6782212 Free PMC article.

8

X-linked mental retardation with macro-orchidism and marker-X chromosomes.

Martin RH, Lin CC, Mathies BJ, Lowry RB. Martin RH, et al. Among authors: lin cc. Am J Med Genet. 1980;7(4):433-41. doi: 10.1002/ajmg.1320070405. Am J Med Genet. 1980. PMID: 6938132

9

Familial complex chromosomal rearrangement resulting in duplication/deletion of 6q14 to 6q16.

Roland B, Lowry RB, Cox DM, Ferreira P, Lin CC. Roland B, et al. Among authors: lin cc. Clin Genet. 1993 Mar;43(3):117-21. doi: 10.1111/j.1399-0004.1993.tb04434.x. Clin Genet. 1993. PMID: 8500257

10

Tertiary trisomy (22q11q),47,+der(22),t(11;22).

Biederman BM, Lin CC, Lowry RB, Somerville R. Biederman BM, et al. Among authors: lin cc. Hum Genet. 1980 Feb;53(2):173-7. doi: 10.1007/BF00273491. Hum Genet. 1980. PMID: 7358384

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