Literature DB >> 13824672

A note on race-specific congenital malformation rates.

T M FRAZIER.   

Abstract

Keywords:  ABNORMALITIES

Mesh:

Year:  1960        PMID: 13824672     DOI: 10.1016/s0002-9378(16)36439-0

Source DB:  PubMed          Journal:  Am J Obstet Gynecol        ISSN: 0002-9378            Impact factor:   8.661


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  8 in total

1.  Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13.3-q21.2 and screening of the candidate genes.

Authors:  Sulman Basit; Syed Kamran-ul-Hassan Naqvi; Muhammad Ansar; Wasim Ahmad
Journal:  Hum Genet       Date:  2011-08-30       Impact factor: 4.132

2.  Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis.

Authors:  U Radhakrishna; J L Blouin; H Mehenni; U C Patel; M N Patel; J V Solanki; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

3.  Polydactyly in American negroes and whites.

Authors:  C M Woolf; N C Myrianthopoulos
Journal:  Am J Hum Genet       Date:  1973-07       Impact factor: 11.025

4.  Polydactyly: a genetic study in South America.

Authors:  E Castilla; J Paz; O Mutchinick; E Muñoz; E Giorgiutti; Z Gelman
Journal:  Am J Hum Genet       Date:  1973-07       Impact factor: 11.025

5.  A genetic study of polydactyly in Utah.

Authors:  C M Woolf; R M Woolf
Journal:  Am J Hum Genet       Date:  1970-01       Impact factor: 11.025

6.  The prevalence of congenital orthopaedic anomalies in a rural community.

Authors:  R L Mittal; A S Sekhon; G Singh; H Thakral
Journal:  Int Orthop       Date:  1993       Impact factor: 3.075

7.  A simple method for testing two-locus models of inheritance.

Authors:  D A Greenberg
Journal:  Am J Hum Genet       Date:  1981-07       Impact factor: 11.025

8.  Isolated heptadactylia: A case report of central polydactyly of the foot.

Authors:  Nicolas Piette; Pierre-Yves Zambelli; Daniel N'Dele
Journal:  Medicine (Baltimore)       Date:  2017-10       Impact factor: 1.889

  8 in total

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