Chen H - Search Results

1

Familial partial trisomy 6q syndromes resulting from inherited ins (5;6) (q33;q15q27).

Chen H, Tyrkus M, Cohen F, Woolley PV Jr, Mayeda K, Bhogaonker A, Espirtu CE, Simpson W. Chen H, et al. Clin Genet. 1976 Jun;9(6):631-7. doi: 10.1111/j.1399-0004.1976.tb01625.x. Clin Genet. 1976. PMID: 1277576

2

Double aneuploidy: partial trisomy 21 and XO/XXX in a family with 12/21 translocation.

Chen H, Tyrkus M, Woolley PV. Chen H, et al. Ann Genet. 1978 Sep;21(3):177-80. Ann Genet. 1978. PMID: 315194

3

An extra small metacentric chromosome identified as a deleted chromosome no. 17.

Palutke W, Chen H, Woolley P Jr, Espiritu C, Vogel HL, Gohle N, Tyrkus M. Palutke W, et al. Among authors: chen h. Clin Genet. 1976 May;9(5):454-58. doi: 10.1111/j.1399-0004.1976.tb01596.x. Clin Genet. 1976. PMID: 1269167

4

Mesomelic dwarfism as the homozygous expression of dyschondrosteosis.

Espiritu C, Chen H, Woolley PV Jr. Espiritu C, et al. Among authors: chen h. Am J Dis Child. 1975 Mar;129(3):375-7. doi: 10.1001/archpedi.1975.02120400075020. Am J Dis Child. 1975. PMID: 1121969 No abstract available.

5

Probable homozygosity for the dyschondrosteosis genes.

Espiritu CE, Chen H, Woolley PV Jr. Espiritu CE, et al. Among authors: chen h. Birth Defects Orig Artic Ser. 1975;11(6):127-32. Birth Defects Orig Artic Ser. 1975. PMID: 1201337 No abstract available.

6

A developmental assessment chart for non-institutionalized Down syndrome children.

Chen H, Woolley PV Jr. Chen H, et al. Growth. 1978 Jun;42(2):157-65. Growth. 1978. PMID: 150361

7

Inter-nipple distance in normal children from birth to 14 years, and in children with Turner's, Noonan's, Down's and other aneuploides.

Chen H, Espiritu C, Casquejo C, Boriboon K, Woolley P Jr. Chen H, et al. Growth. 1974 Dec;38(4):421-36. Growth. 1974. PMID: 4282364 No abstract available.

8

Omphalocele and partial trisomy 1q syndrome.

Chen H, Gershanik JJ, Mailhes JB, Sanusi ID. Chen H, et al. Hum Genet. 1979;53(1):1-4. doi: 10.1007/BF00289442. Hum Genet. 1979. PMID: 535894

9

Triploidy syndrome. A report on two live-born (69, XXY) and one still-born (69, XXX) infants.

Saadi AA, Juliar JF, Harm J, Brough AJ, Perrin EV, Chen H. Saadi AA, et al. Among authors: chen h. Clin Genet. 1976 Jan;9(1):43-50. doi: 10.1111/j.1399-0004.1976.tb01548.x. Clin Genet. 1976. PMID: 174849

10

Mosaic trisomy 19 syndrome.

Chen H, Yu CW, Wood MJ, Landry K. Chen H, et al. Ann Genet. 1981;24(1):32-3. Ann Genet. 1981. PMID: 6971614

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