scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1032294651 |
P356 | DOI | 10.1007/BF00291316 |
P698 | PubMed publication ID | 669715 |
P2093 | author name string | J. Schwarz | |
R. A. Pfeiffer | |||
E. Kessel | |||
W. Blanke | |||
P2860 | cites work | Terminal (1)(q43) long-arm deletion of chromosome no. 1 in a three-year-old female | Q41937235 |
Ring-1 chromosome, microcephalic dwarfism, and acute myeloid leukemia | Q41937914 | ||
RING-1 CHROMOSOME AND MICROCEPHALIC DWARFISM | Q41939552 | ||
Primary hypothyroidism, growth hormone deficiency and congenital malformations in a child with the karyotype 46,XY,del(1)(q25q32). | Q44607080 | ||
Partial trisomy of the long arm of human chromosome 1 as demostrated by in situ hybridization with 5S ribosomal RNA | Q45019161 | ||
[De novo interstitial deletion Del (1) (q24 q32.1) in a malformed child] | Q69148617 | ||
Ring 1 chromosome and dwarfism—a possible syndrome | Q72299227 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | chromosomal deletion syndrome | Q16918398 |
human chromosomes 1-3 | Q70192437 | ||
P304 | page(s) | 333-337 | |
P577 | publication date | 1978-06-01 | |
1978-06-27 | |||
P1433 | published in | Human Genetics | Q5937167 |
P1476 | title | Terminal deletion of the long arm of chromosome 1 in a malformed newborn | |
P478 | volume | 42 |
Q69802596 | Chromosomes of human sperm: variability among normal individuals |
Q50306046 | Neurological aspects of del(1q) syndrome |
Q35201447 | New deletion syndrome: 1q43 |
Q41209155 | Similarities of EEG and seizures in del(1q) and benign rolandic epilepsy |
Q41684207 | Terminal long-arm deletion of chromosome 1 in a male infant |
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