Literature DB >> 6082902

A sex chromatin survey of newborn children in two London hospitals.

A I Taylor, E C Moores.   

Abstract

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Year:  1967        PMID： 6082902      PMCID： PMC1468554          DOI： 10.1136/jmg.4.4.258

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  7 in total

1.  LIPOID ADRENAL HYPERPLASIA.

Authors:  N J O'DOHERTY
Journal:  Guys Hosp Rep       Date:  1964

2.  SEX-CHROMOSOME ABNORMALITIES IN NEWBORN BABIES.

Authors:  N MACLEAN; D G HARNDEN; W M BROWN; J BOND; D J MANTLE
Journal:  Lancet       Date:  1964-02-08       Impact factor: 79.321

3.  CONGENITAL ANOMALIES IN THE NEWBORN INFANT, INCLUDING MINOR VARIATIONS. A STUDY OF 4,412 BABIES BY SURFACE EXAMINATION FOR ANOMALIES AND BUCCAL SMEAR FOR SEX CHROMATIN.

Authors:  P M MARDEN; D W SMITH; M J MCDONALD
Journal:  J Pediatr       Date:  1964-03       Impact factor: 4.406

4.  CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). I. DATA ON A CONSECUTIVE SERIES OF PATIENTS REFERRED FOR GENETIC COUNSELLING AND DIAGNOSIS.

Authors:  J L HAMERTON; F GIANNELLI; P E POLANI
Journal:  Cytogenetics       Date:  1965

5.  [Comparison of the phenotype and nuclear morphological sex in 3029 newborn infants].

Authors:  B WIESLI
Journal:  Acta Anat (Basel)       Date:  1962

6.  Sex reversal in newborn babies.

Authors:  K L MOORE
Journal:  Lancet       Date:  1959-01-31       Impact factor: 79.321

Review 7.  Patau's, Edwards' and Cri du Chat syndromes: a tabulated summary of current findings.

Authors:  A I Taylor
Journal:  Dev Med Child Neurol       Date:  1967-02       Impact factor: 5.449
  7 in total
  11 in total

1.  Prevalence of Edwards' syndrome. Clustering and seasonal variation?

Authors:  J Nielsen; V Holm; J Haahr
Journal:  Humangenetik       Date:  1975

2.  Male pseudohermaphroditism in a child with Down's syndrome.

Authors:  M S Golbus; C J Beauchamp; F A Conte
Journal:  J Med Genet       Date:  1973-06       Impact factor: 6.318

Review 3.  Down's syndrome. Current stage of cytogenetic research.

Authors:  M Mikkelsen
Journal:  Humangenetik       Date:  1971

4.  Sex chromatin and chromosome abnormalities among 10,412 liveborn babies.

Authors:  S N Pantelakis; O M Chryssostomidou; D Alexiou; T Valaes; S A Doxiadis
Journal:  Arch Dis Child       Date:  1970-02       Impact factor: 3.791

5.  Double aneuploidy: the frequency of XXY in males with Down's syndrome.

Authors:  F Hecht; J E Nievaard; N Duncanson; J R Miller; J V Higgins; W J Kimberling; F A Walker; G S Smith; H C Thuline; B Tischler
Journal:  Am J Hum Genet       Date:  1969-07       Impact factor: 11.025

6.  A case of double aneuploidy, 47,XXY,14-,t(13q14q)+, also probably homozygous for the cystic fibrosis gene.

Authors:  R H Lindenbaum; N L Blackwell; D J De Sa'
Journal:  J Med Genet       Date:  1972-06       Impact factor: 6.318

7.  Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome.

Authors:  A I Taylor
Journal:  J Med Genet       Date:  1968-09       Impact factor: 6.318

8.  The triplo-X female: an appraisal based on a study of 12 cases and a review of the literature.

Authors:  M L Barr; F R Sergovich; D H Carr; E L Saver
Journal:  Can Med Assoc J       Date:  1969-09-06       Impact factor: 8.262

9.  Uveal coloboma and true Klinefelter syndrome.

Authors:  J François; M T Leuven; P Gombault
Journal:  J Med Genet       Date:  1970-09       Impact factor: 6.318

10.  Three chromosome abnormalities (trisomy 21, XXY, and a de nova reciprocal translocation) in a child with 48, XXY, + 21,T(6;10)(P22-24;P12).

Authors:  P D Buchanan
Journal:  Humangenetik       Date:  1975-08-25
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