PubMed (OMIM) for id: 763392

Year	Number of Results
1968	1
1970	1
1974	1
1975	1
1980	2
1983	1
2002	1
2024	0

1

Identification and molecular characterization of two closely related G protein-coupled receptors activated by prokineticins/endocrine gland vascular endothelial growth factor.

Lin DC, Bullock CM, Ehlert FJ, Chen JL, Tian H, Zhou QY. Lin DC, et al. J Biol Chem. 2002 May 31;277(22):19276-80. doi: 10.1074/jbc.M202139200. Epub 2002 Mar 8. J Biol Chem. 2002. PMID: 11886876 Free article.

2

Lack of close linkage of hypogonadotropic hypogonadism with HLA.

Dornan J, Barnard JM, Farid NR. Dornan J, et al. Tissue Antigens. 1980 May;15(5):510-1. doi: 10.1111/j.1399-0039.1980.tb00217.x. Tissue Antigens. 1980. PMID: 7444936 No abstract available.

3

Female Kallmann's syndrome: evidence for a hypothalamic luteinizing hormone-releasing hormone deficiency.

Soules MR, Hammond CB. Soules MR, et al. Fertil Steril. 1980 Jan;33(1):82-5. doi: 10.1016/s0015-0282(16)44484-5. Fertil Steril. 1980. PMID: 6985875 Free article. No abstract available.

4

The syndrome of anosmia with hypogonadotropic hypogonadism: a genetic study of 18 new families and a review.

White BJ, Rogol AD, Brown KS, Lieblich JM, Rosen SW. White BJ, et al. Am J Med Genet. 1983 Jul;15(3):417-35. doi: 10.1002/ajmg.1320150307. Am J Med Genet. 1983. PMID: 6881209

5

Hypogonadotropic hypogonadism associated with anosmia in the female.

Tagatz G, Fialkow PJ, Smith D, Spadoni L. Tagatz G, et al. N Engl J Med. 1970 Dec 10;283(24):1326-9. doi: 10.1056/NEJM197012102832407. N Engl J Med. 1970. PMID: 5478454 No abstract available.

6

Familial holoprosencephaly with endocrine dysgenesis.

Hintz RL, Menking M, Sotos JF. Hintz RL, et al. J Pediatr. 1968 Jan;72(1):81-7. doi: 10.1016/s0022-3476(68)80403-2. J Pediatr. 1968. PMID: 4294576 No abstract available.

7

Cryptorchidism in a family with Kallmann's syndrome.

Turner RC, Bobrow LG, MacKinnon PC, Bonnar J, Hockaday TD, Ellis JD. Turner RC, et al. Proc R Soc Med. 1974 Jan;67(1):33-5. Proc R Soc Med. 1974. PMID: 4150739 Free PMC article. No abstract available.

8

Familial Kallmann syndrome with unilateral renal aplasia.

Wegenke JD, Uehling DT, Wear JB Jr, Gordon ES, Bargman JG, Deacon JS, Herrmann JP, Opitz JM. Wegenke JD, et al. Clin Genet. 1975 May-Jun;7(5):368-81. doi: 10.1111/j.1399-0004.1975.tb00344.x. Clin Genet. 1975. PMID: 1080088

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