Hirschhorn K - Search Results

1

Deceleration of intellectual development in a XXXXY child: a follow-up.

Shapiro LR, Brill CB, Hsu LY, Calvin ME, Hirschhorn K. Shapiro LR, et al. Among authors: hirschhorn k. Am J Dis Child. 1971 Aug;122(2):163-4. doi: 10.1001/archpedi.1971.02110020097015. Am J Dis Child. 1971. PMID: 5564160 No abstract available.

2

XXXXY boy. A 15-month-old child with normal intellectual development.

Shapiro LR, Hsu LY, Calvin ME, Hirschhorn K. Shapiro LR, et al. Among authors: hirschhorn k. Am J Dis Child. 1970 Jan;119(1):79-81. Am J Dis Child. 1970. PMID: 5410298 No abstract available.

3

Neonatal Klinefelter's syndrome.

Edlow JB, Shapiro LR, Hsu LY, Hirschhorn K. Edlow JB, et al. Among authors: hirschhorn k. Am J Dis Child. 1969 Nov;118(5):788-91. doi: 10.1001/archpedi.1969.02100040790021. Am J Dis Child. 1969. PMID: 5348380 No abstract available.

4

47,XXY-48,XXXY-49,XXXXY mosaicism in a 4-year-old child.

Kardon NB, Beratis NG, Hsu LY, Moloshok RE, Hirschhorn K. Kardon NB, et al. Among authors: hirschhorn k. Am J Dis Child. 1971 Aug;122(2):160-2. Am J Dis Child. 1971. PMID: 5564159 No abstract available.

5

Prenatal diagnosis of trisomy 18. Pathologic findings in 20-week conceptus.

Hsu LY, Strauss L, Dubin E, Hirschhorn K. Hsu LY, et al. Among authors: hirschhorn k. Am J Dis Child. 1973 Feb;125(2):290-2. doi: 10.1001/archpedi.1973.04160020098020. Am J Dis Child. 1973. PMID: 4685842 No abstract available.

6

Prenatal diagnosis of double trisomy.

Hsu LY, Strauss L, Alter AV, Kim HJ, Hirschhorn K. Hsu LY, et al. Among authors: hirschhorn k. Am J Dis Child. 1975 Mar;129(3):381-2. doi: 10.1001/archpedi.1975.02120400079021. Am J Dis Child. 1975. PMID: 123706 No abstract available.

7

Supernumerary small ring chromosome.

Kaffe S, Kim HJ, Hsu LY, Brill CB, Hirschhorn K. Kaffe S, et al. Among authors: hirschhorn k. J Med Genet. 1977 Dec;14(6):447-51. doi: 10.1136/jmg.14.6.447. J Med Genet. 1977. PMID: 604496 Free PMC article.

8

The syndrome of ectrodactyly, ectodermal dysplasia and cleft lip and palate: report of a family demonstrating a dominant inheritance pattern.

Brill CB, Hsu LY, Hirschhorn K. Brill CB, et al. Among authors: hirschhorn k. Clin Genet. 1972;3(5):295-302. doi: 10.1111/j.1399-0004.1972.tb01461.x. Clin Genet. 1972. PMID: 5084380 No abstract available.

9

Unusual Turner mosaicism (45,X-47,XXX;45,X-46,XXqi;45,X-46,XXr): detection through deceleration from mormal linear growth or secondary amenorrhea.

Hsu LY, Hirschhorn K. Hsu LY, et al. Among authors: hirschhorn k. J Pediatr. 1971 Aug;79(2):276-81. doi: 10.1016/s0022-3476(71)80113-0. J Pediatr. 1971. PMID: 5560050 No abstract available.

10

Klinefelter's syndrome in identical twins with the 46,XX chromosome constitution.

Nicolis GL, Hsu LY, Sabetghadam R, Kardon NB, Chernay PR, Mathur DP, Rose HG, Hirschhorn K, Gabrilove JL. Nicolis GL, et al. Among authors: hirschhorn k. Am J Med. 1972 Apr;52(4):482-91. doi: 10.1016/0002-9343(72)90039-3. Am J Med. 1972. PMID: 5017243 No abstract available.

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