This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

. 1964 Jul 2:271:12-6.

doi: 10.1056/NEJM196407022710102.

FAMILIAL CHROMOSOME-2, 3 TRANSLOCATION ASCERTAINED THROUGH AN INFANT WITH MULTIPLE MALFORMATIONS

C S LEE, P BOWEN, H ROSENBLUM, L LINSAO

PMID: 14148222
DOI: 10.1056/NEJM196407022710102

FAMILIAL CHROMOSOME-2, 3 TRANSLOCATION ASCERTAINED THROUGH AN INFANT WITH MULTIPLE MALFORMATIONS

C S LEE et al. N Engl J Med. 1964.

. 1964 Jul 2:271:12-6.

doi: 10.1056/NEJM196407022710102.

Authors

C S LEE, P BOWEN, H ROSENBLUM, L LINSAO

PMID: 14148222
DOI: 10.1056/NEJM196407022710102

No abstract available

PubMed Disclaimer

Similar articles

MALFORMATIONS OF THE EAR AS A CLUE TO UROGENITAL ANOMALIES. REPORT OF SIX ADDITIONAL CASES.
LONGENECKER CG, RYAN RF, VINCENT RW. LONGENECKER CG, et al. Plast Reconstr Surg. 1965 Mar;35:303-9. doi: 10.1097/00006534-196503000-00007. Plast Reconstr Surg. 1965. PMID: 14261988 No abstract available.
CONGENITAL MALFORMATIONS. CLINICAL AND COMMUNITY CONSIDERATIONS.
INGALLS TH, KLINGBERG MA. INGALLS TH, et al. Am J Med Sci. 1965 Mar;249:316-44. doi: 10.1097/00000441-196503000-00011. Am J Med Sci. 1965. PMID: 14273322 Review. No abstract available.
HOLOPROSENCEPHALY: A CASE REPORT WITH NO EXTRACRANIAL ABNORMALITIES AND NORMAL CHROMOSOME COUNT AND KARYOTYPE.
BISHOP K, CONNOLLY JM, CARTER CH, CARPENTER DG. BISHOP K, et al. J Pediatr. 1964 Sep;65:406-14. doi: 10.1016/s0022-3476(64)80405-4. J Pediatr. 1964. PMID: 14210861 No abstract available.
[TRISOMY D1(13-15) AS CAUSE OF MULTIPLE MALFORMATIONS].
TELLER W, PFEIFFER RA. TELLER W, et al. Z Kinderheilkd. 1964 Feb 14;89:36-48. Z Kinderheilkd. 1964. PMID: 14168965 German. No abstract available.
"Newer" facial clefting syndromes.
Gorlin RJ, Cervenka J, Cohen MM Jr. Gorlin RJ, et al. Birth Defects Orig Artic Ser. 1977;13(3B):1-9. Birth Defects Orig Artic Ser. 1977. PMID: 329913 Review. No abstract available.

See all similar articles

Cited by

[Familial 2-C translocation: 46,XYt(2p-;Cp+) and 46,XXCp+].
Bender K, Reinwein H, Gorman LZ, Wolf U. Bender K, et al. Humangenetik. 1969 Oct;8(2):94-104. doi: 10.1007/BF00295832. Humangenetik. 1969. PMID: 5365588 German. No abstract available.
New chromosomal dysmorphic syndromes. 3. Partial trisomy 3q.
Stengel-Rutkowski S, Murken JD, Pilar V, Dutrillaux B, Rodewald A, Goebel R, Bassermann R. Stengel-Rutkowski S, et al. Eur J Pediatr. 1979 Feb 8;130(2):111-25. doi: 10.1007/BF00442348. Eur J Pediatr. 1979. PMID: 421691
Congenital chromosomal syndromes. A model for pathogenesis.
Rohde RA. Rohde RA. Calif Med. 1965 Oct;103(4):249-53. Calif Med. 1965. PMID: 5318572 Free PMC article. Review.
Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).
Allderdice PW, Browne N, Murphy DP. Allderdice PW, et al. Am J Hum Genet. 1975 Nov;27(6):699-718. Am J Hum Genet. 1975. PMID: 1200027 Free PMC article.
Congenital malformations of the central nervous system in spontaneous abortions.
Creasy MR, Alberman ED. Creasy MR, et al. J Med Genet. 1976 Feb;13(1):9-16. doi: 10.1136/jmg.13.1.9. J Med Genet. 1976. PMID: 775092 Free PMC article.

MeSH terms

Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions

LinkOut - more resources

Full Text Sources
- Atypon
- Ovid Technologies, Inc.