Terminal deletion of the long arm of chromosome 1 in a malformed newborn

scientific article published on June 27, 1978

Terminal deletion of the long arm of chromosome 1 in a malformed newborn is …
instance of (P31):
scholarly articleQ13442814

External links are
P6179Dimensions Publication ID1032294651
P356DOI10.1007/BF00291316
P698PubMed publication ID669715

P2093author name stringJ. Schwarz
R. A. Pfeiffer
E. Kessel
W. Blanke
P2860cites workTerminal (1)(q43) long-arm deletion of chromosome no. 1 in a three-year-old femaleQ41937235
Ring-1 chromosome, microcephalic dwarfism, and acute myeloid leukemiaQ41937914
RING-1 CHROMOSOME AND MICROCEPHALIC DWARFISMQ41939552
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 RNAQ45019161
[De novo interstitial deletion Del (1) (q24 q32.1) in a malformed child]Q69148617
Ring 1 chromosome and dwarfism—a possible syndromeQ72299227
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectchromosomal deletion syndromeQ16918398
human chromosomes 1-3Q70192437
P304page(s)333-337
P577publication date1978-06-01
1978-06-27
P1433published inHuman GeneticsQ5937167
P1476titleTerminal deletion of the long arm of chromosome 1 in a malformed newborn
P478volume42

Reverse relations

cites work (P2860)
Q69802596Chromosomes of human sperm: variability among normal individuals
Q50306046Neurological aspects of del(1q) syndrome
Q35201447New deletion syndrome: 1q43
Q41209155Similarities of EEG and seizures in del(1q) and benign rolandic epilepsy
Q41684207Terminal long-arm deletion of chromosome 1 in a male infant

Search more.