Literature DB >> 7239511

Monosomy 1pter.

E Yunis, L Quintero, M Leibovici.   

Abstract

Mesh：

Year:  1981        PMID： 7239511     DOI： 10.1007/bf00274679

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


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  9 in total

1.  A cytogenetic study of human spontaneous abortions using banding techniques.

Authors:  M R Creasy; J A Crolla; E D Alberman
Journal:  Hum Genet       Date:  1976-02-29       Impact factor: 4.132

2.  Partial trisomy 1 due to a "shift" and probable location of the Duffy (Fy) locus.

Authors:  C G Palmer; J C Christian; A D Merritt
Journal:  Am J Hum Genet       Date:  1977-07       Impact factor: 11.025

3.  Trisomy of the long arm of human chromosome 1.

Authors:  T H Norwood; H Hoehn
Journal:  Humangenetik       Date:  1974

4.  Partial Trisomy 1, Karyotype 46,XY,12-,t(1q,12p)+.

Authors:  H Van den Berghe; M Van Eygen; J P Fryns; W Tanghe; H Verresen
Journal:  Humangenetik       Date:  1973-05-25

5.  A partial trisomy of chromosome 1 in a family with a t(1q-;4q+) translocation.

Authors:  R L Neu; L I Gardner
Journal:  Clin Genet       Date:  1973-06       Impact factor: 4.438

6.  "De novo" trisomy 1q32 leads to 1qter and monosomy 3p25 leads to 3pter.

Authors:  E Yunis; H Egel; R Zúñiga; E Ramirez; O M Torres de Caballero; M Leibovici
Journal:  Hum Genet       Date:  1977-04-07       Impact factor: 4.132

7.  Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh.

Authors:  M L Rivas; P M Conneally; F Hecht; E W Lovrien; E Magenis; A D Merritt; D A Meyers; C G Palmer; L Wang
Journal:  Birth Defects Orig Artic Ser       Date:  1975

8.  Abnormalities of chromosome 1 in myeloproliferative disorders.

Authors:  J D Rowley
Journal:  Cancer       Date:  1975-11       Impact factor: 6.860

9.  Mapping human autosomes: evidence supporting assignment of rhesus to the short arm of chromosome No. 1.

Authors:  W L Marsh; R S Chaganti; F H Gardner; K Mayer; P C Nowell; J German
Journal:  Science       Date:  1974-03-08       Impact factor: 47.728
  9 in total
  7 in total

1.  Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.

Authors:  S K Shapira; C McCaskill; H Northrup; A S Spikes; F F Elder; V R Sutton; J R Korenberg; F Greenberg; L G Shaffer
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

2.  Clinical consequences of deletion 1p35.

Authors:  S L Wenger; M W Steele; D J Becker
Journal:  J Med Genet       Date:  1988-04       Impact factor: 6.318

Review 3.  Monosomy 1p36.

Authors:  A Slavotinek; L G Shaffer; S K Shapira
Journal:  J Med Genet       Date:  1999-09       Impact factor: 6.318

4.  A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1.

Authors:  N Abbas; G Novelli; N C Stella; O Triolo; F Corrado; M Fellous; M Chery; S Gilgenkrantz; B Dallapiccola
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

5.  Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes.

Authors:  K M Keppler-Noreuil; A J Carroll; W H Finley; S L Rutledge
Journal:  J Med Genet       Date:  1995-08       Impact factor: 6.318

6.  Interstitial deletion 1p in a 30 year old woman.

Authors:  M B Petersen; M Warburg
Journal:  J Med Genet       Date:  1987-04       Impact factor: 6.318

7.  1p36 deletion syndrome: first case report in Morocco detected by fluorescence in situ hybridization.

Authors:  Kenza Dafir; Fatima Zahra Bouzid; Maria Mansouri; Nisrine Aboussair
Journal:  Pan Afr Med J       Date:  2020-12-16
  7 in total

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