Literature DB >> 2378627

Growth hormone deficiency in children with chromosomal abnormalities.

H P Schwarz, S C Duck.   

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Year:  1990        PMID： 2378627      PMCID： PMC1792267          DOI： 10.1136/adc.65.3.334-a

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  4 in total

1.  Ring 21 chromosome: the mild end of the phenotypic spectrum.

Authors:  R J Gardner; N A Monk; J E Clarkson; G J Allen
Journal:  Clin Genet       Date:  1986-12       Impact factor: 4.438

2.  Clinical and chromosomal studies of the 18q- syndrome.

Authors:  W Wertelecki; P S Gerald
Journal:  J Pediatr       Date:  1971-01       Impact factor: 4.406

3.  A male infant with holoprosencephaly, associated with ring chromosome 21.

Authors:  D C Aronson; M C Jansweijer; J M Hoovers; P G Barth
Journal:  Clin Genet       Date:  1987-01       Impact factor: 4.438

4.  Growth hormone, suspected gonadotrophin deficiency, and ring 18 chromosome.

Authors:  S S Abusrewil; A McDermott; D C Savage
Journal:  Arch Dis Child       Date:  1988-09       Impact factor: 3.791
  4 in total
  2 in total

1.  Growth hormone deficiency in children with chromosomal abnormalities.

Authors:  D P Davies
Journal:  Arch Dis Child       Date:  1990-10       Impact factor: 3.791

Review 2.  Clinical Characteristics and Long-Term Recombinant Human Growth Hormone Treatment of 18q- Syndrome: A Case Report and Literature Review.

Authors:  Shanshan Liu; Meiping Chen; Hongbo Yang; Shi Chen; Linjie Wang; Lian Duan; Huijuan Zhu; Hui Pan
Journal:  Front Endocrinol (Lausanne)       Date:  2021-12-09       Impact factor: 5.555
  2 in total

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