✦ LIBER ✦

Carbonic anhydrase in the utero-vaginal junction of immature and mature ostriches

✍ Scribed by Holm, L.; Ruziwa, S.D.; Dantzer, V.; Ridderstrale, Y.

Book ID: 126705665
Publisher: Taylor and Francis Group
Year: 2000
Tongue: English
Weight: 289 KB
Volume: 41
Category: Article
ISSN: 0007-1668
DOI: 10.1080/713654906

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A splice junction mutation in intron 2 o

A splice junction mutation in intron 2 of the carbonic anhydrase II gene of osteopetrosis patients from Arabic countries

✍ Peiyi Y. Hu; Donna E. Roth; Laura A. Skaggs; Patrick J. Venta; Richard E. Tashia 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 438 KB

Clinical manifestations in patients with carbonic anhydrase (CA) I1 deficiency include osteopetrosis, renal tubular acidosis, and cerebral calcification. Of the 39 reported cases of the carbonic anhydrase I1 deficiency syndrome, 72% were patients from North African and Middle Eastern countries, most

Early postnatal muscle contractile activ

Early postnatal muscle contractile activity regulates the carbonic anhydrase phenotype of proprioceptive neurons in young and mature mice: Evidence for a critical period in development

✍ V. Mayeux; F. Pons; M. Baldy-Moulinier; J. Valmier 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 938 KB

Successful DNA-based prenatal diagnosis

Successful DNA-based prenatal diagnosis of the 728+1 g→t mutation at the exon 6-intron 6 junction in the carbonic anhydrase II gene

✍ M. Rafiq Islam; Pietro Strisciuglio; Giuseppe Bonapace; William S. Sly 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 146 KB 👁 1 views

and three siblings (aged 17, 20 and 22 years) also had an elongated chromosome 16 short arm. During counselling, the parents were informed of the familial nature of the anomaly. They were informed that the cytogenetic characterization of the chromosome 16 anomaly and the information derived from pre