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1. FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA.

Authors: I A UCHIDA; K N MCRAE; M RAY
Journal: Am J Hum Genet Date: 1965-09 Impact factor: 11.025

2. Ring chromosome 18 in a patient with multiple anomalies.

Authors: C G Palmer; N Fareed; A D Merritt
Journal: J Med Genet Date: 1967-06 Impact factor: 6.318

3. Short arm deletions in group E and chromosomal "deletion" syndromes.

Authors: B R Migeon
Journal: J Pediatr Date: 1966-09 Impact factor: 4.406

4. Partial 18 monosomy in the cyclops malformation.

Authors: H M Nitowsky; N Sindhvananda; U R Konigsberg; T Weinberg
Journal: Pediatrics Date: 1966-02 Impact factor: 7.124

4 in total

2 in total

1. Cytogenetic analysis in congenital hypothyroidism.

Authors: F Uccellatore; L Sava; D Giuffrida; T Fazio; F Calaciura; C Regalbuto; R Vigneri
Journal: J Endocrinol Invest Date: 1990 Jul-Aug Impact factor: 4.256

2. Hypothyroidism and levothyroxine-responsive liver dysfunction in a patient with ring chromosome 18 syndrome.

Authors: Kazuhiro Ohkubo; Kenji Ihara; Shouichi Ohga; Masataka Ishimura; Toshiro Hara
Journal: Thyroid Date: 2012-09-04 Impact factor: 6.568

2 in total