[3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME]
[Article in
French]
- PMID: 14095841
Item in Clipboard
[3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME]
[Article in
French]
C R Hebd Seances Acad Sci.
.
No abstract available
Similar articles
-
A CASE OF XXXXY SEX CHROMOSOME ANOMALY WITH AUTORADIOGRAPHIC STUDIES.Cytogenetics. 1963;2:208-31. doi: 10.1159/000129780. Cytogenetics. 1963. PMID: 14104167 No abstract available.
-
ENLARGED CHROMOSOMAL SATELLITES ASSOCIATED WITH MENTAL RETARDATION AND DIGITAL ARCHES IN THREE GENERATIONS.Ann Hum Genet. 1964 Sep;28:21-6. doi: 10.1111/j.1469-1809.1964.tb00456.x. Ann Hum Genet. 1964. PMID: 14204849 No abstract available.
-
FAMILIAL CHROMOSOME-2, 3 TRANSLOCATION ASCERTAINED THROUGH AN INFANT WITH MULTIPLE MALFORMATIONS.N Engl J Med. 1964 Jul 2;271:12-6. doi: 10.1056/NEJM196407022710102. N Engl J Med. 1964. PMID: 14148222 No abstract available.
-
OCULOAURICULOVERTEBRAL DYSPLASIA.J Pediatr. 1963 Nov;63:991-9. doi: 10.1016/s0022-3476(63)80233-4. J Pediatr. 1963. PMID: 14071056 Review. No abstract available.
-
[External ear abnormalities: syndromic and genetic aspects].Rev Laryngol Otol Rhinol (Bord). 1997;118(1):5-10. Rev Laryngol Otol Rhinol (Bord). 1997. PMID: 9206298 Review. French.
Cited by
-
Cri du chat syndrome patients have DNA methylation changes in genes linked to symptoms of the disease.Clin Epigenetics. 2022 Oct 14;14(1):128. doi: 10.1186/s13148-022-01350-3. Clin Epigenetics. 2022. PMID: 36242045 Free PMC article.
-
Functional implications of differential chromosome banding.Am J Hum Genet. 1975 Sep;27(5):676-85. Am J Hum Genet. 1975. PMID: 51585 Free PMC article.
-
Chromosome mosaicism in a child with features characteristic of the 'Cat Cry' syndrome.J Med Genet. 1966 Mar;3(1):66-9. doi: 10.1136/jmg.3.1.66. J Med Genet. 1966. PMID: 5911836 Free PMC article. No abstract available.
-
Clinical and molecular characterization of 12 prenatal cases of Cri-du-chat syndrome.Mol Genet Genomic Med. 2020 Aug;8(8):e1312. doi: 10.1002/mgg3.1312. Epub 2020 Jun 4. Mol Genet Genomic Med. 2020. PMID: 32500674 Free PMC article.
-
Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.Humangenetik. 1973 Mar 23;18(1):16-32. doi: 10.1007/BF00279027. Humangenetik. 1973. PMID: 4578677 Review. No abstract available.